{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5132181007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4629507007,"location":{"name":"Foster City"},"metadata":null,"id":5132181007,"updated_at":"2026-06-01T19:31:43-04:00","requisition_id":"2026-REP-019","title":"AP Accountant","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-07T17:17:51-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a detail-oriented and highly organized AP Accountant to join our Accounting Operations team. This role is responsible for the accurate and timely processing of accounts payable transactions, expense reports, vendor communications, and related general accounting activities. The ideal candidate will thrive in a dynamic, complex, and fast-paced environment and possess strong analytical, organizational, customer service and critical thinking skills. This position requires a combination of technical accounting knowledge and operational experience, along with the ability to independently resolve issues, manage multiple priorities, and collaborate effectively across departments. The candidate should be able self-motivated, adaptable, and a strong team player with a solid work ethic. This role regularly interfaces with internal stakeholders and external vendors and plays a critical role in supporting the Finance and Accounting organization within a growing company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Responsible for processing high volumes of accounts payable transactions, including invoice entry, account coding, and ensuring proper accounting period entry for accuracy and compliance with company policies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review invoices for appropriate supporting documentation prior to processing and payment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Process accounts payable by matching invoices with appropriate purchase orders and supporting documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review vendor contracts and exercise judgment in assigning appropriate expense accounts, departments, and project coding for non-PO invoices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Research and resolve vendor account, invoice, and payment discrepancies while maintaining accounts payable in good standing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage and monitor the AP email inbox, including responding to vendor inquiries, payment requests, and invoice related questions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure adherence to company signature authority and approval policies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the Concur expense reporting system, including expense report processing, audits and user support.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review employee expense reports thoroughly to ensure compliance with company policies and procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review expense reports containing Healthcare Professional (HCP) related expenses to ensure Sunshine Act compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the expense reports email inbox and provide support for employee expense submissions and travel booking inquiries.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide excellent customer service to internal stakeholders and external vendors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support quarterly reviews and annual audit by providing requested documentation to auditors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;System maintenance for tax reporting compliance and year-end processing of 1099’s.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support financial systems implementations and participate in process improvements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist on special projects and ad-hoc assignments as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adapt to evolving responsibilities and business needs within a growing organization.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Accounting, Finance, or related field preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5+ years of Accounts Payable or general accounting experience, preferably in a high-volume environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Required experience with Concur expense management system and NetSuite ERP system.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of AP processes, expense reporting, and internal controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of 1099 reporting requirements and audit support processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in Microsoft Office applications, particularly Excel.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with Sunshine Act compliance is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Knowledge, Skills and Abilities: \u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical, problem solving, and critical thinking skills with the ability to exercise sound judgment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong verbal and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently to complete tasks in an accurate and timely manner while managing multiple priorities in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly organized, detail-oriented, dependable, and committed to producing accurate, high-quality work.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Positive attitude, team-oriented mindset, and willingness to adapt to changing priorities and responsibilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Customer-service oriented with the ability to work collaboratively across departments and with external vendors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to prioritize tasks effectively and seek guidance when needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $115,000 to $130,000USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033156007,"name":"Corporate Functions","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5041343007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4587731007,"location":{"name":"Foster City"},"metadata":null,"id":5041343007,"updated_at":"2026-06-01T19:34:36-04:00","requisition_id":"2026-BUD-027","title":"Associate Director, GCP QA","company_name":"Mirum Pharmaceuticals","first_published":"2026-02-03T11:25:42-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director of GCP/GVP/GLP-QA is responsible for supporting Mirum’s clinical study programs as the GCP-QA representative on the study management team; managing activities involving GCP quality assurance and compliance with applicable regulatory requirements; development and implementation of policies and procedures to ensure quality standards in compliance with relevant regulatory and quality guidelines. Additionally, this position will support GVP and GLP QA operational activities to ensure data integrity and meeting regulatory expectations and industry standards.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position requires experience with global contract research organizations (CROs) and GCP Vendors as well as knowledge of global GCP regulations.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Achieve established timelines for deliverables.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;QA Representative for assigned Mirum’s Program’s Clinical Study Management Teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage/Support BIMO inspection readiness activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support GCP/GCLP/GVP internal audits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide quality oversite for the GCP/GVP/GLP vendor activities, including internal/external deviations, CAPAs, change controls, and KPIs/KQIs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support GCP, GCLP and GVP Vendor Management/Audit Program. Ad hoc audits may be requested.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with planning and supporting Clinical Site Management/Audit Program. Ad hoc site audits may be requested.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with and support regulatory agency inspections for the GCP and PV impacted functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide GCP/GCLP/GVP Training as necessary\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Quality Management Team (QMT) by providing monthly/quarterly updates based on role and responsibilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support process improvement of QA department, KPI/QPI tracking and oversight.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage GCP/GVP/GLP consultant(s) as needed\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s Degree in a scientific discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10-12 years of experience in the pharmaceutical industry, including 5-10 years in GCP Quality and 5+ years supervising GCP Quality internal staff and/or external consultants.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge and demonstrated experience in the applicable GCP regulations, FDA Regulations and Good Clinical Practices, EMA EudraLex Regulations, and ICH Guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong verbal and written communication.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of basic GVP, GCLP and GLP regulations.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $190,000 to $205,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033155007,"name":"Quality Assurance","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5131784007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4629326007,"location":{"name":"Foster City"},"metadata":null,"id":5131784007,"updated_at":"2026-06-01T19:35:52-04:00","requisition_id":"2026-MAY-014","title":"Associate Director, Global Medical Communications ","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-07T14:28:14-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director, Global Medical Communications for the LIVMARLI/Bile Acid Portfolio Global Medical Affairs Team (GMAT) is a critical team role with a high-level of accountability, reporting to the GMAT Lead. This role will focus on developing and executing GMAT materials and initiatives, including development, approval, and roll-out of Field Medical Materials; creation of content for and execution of Medical Advisory Boards; and creation of content for and execution of Scientific Symposia and other Medical Education initiatives. The Associate Director of Medical Communications will collaborate with external Medical Communications agencies and Medical Education partners to create timely, relevant, accurate, and engaging tools and programs that support Mirum scientific and medical objectives. They will also collaborate in the management of the database of Medical Field tools, including updating, archiving, and tracking of existing materials, and strategic planning and development of new tools based on the needs and objectives of the GMAT. Essential to this role is the ability to effectively communicate and work with internal stakeholders and external thought leaders in a fast-paced environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Key Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and update Field Medical Materials, materials for Medical Advisory Boards, and materials for Scientific Symposia and other Medical Education initiatives independently or with guidance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all Medical Materials are timely, relevant, accurate, and engaging; are consistent with Mirum scientific and medical objectives; and meet appropriate Regulatory and Compliance standards for the intended use and audience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate in the management of the database of Medical Field tools, including updating, archiving, and tracking of existing materials and strategic planning and development of new tools based on needs and objectives of the Medical Team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage Medical, Legal, and Regulatory (MLR) Committee submission and review of Medical Materials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organize Medical Advisory Board meetings including operational planning for advisory boards (contracting with advisors, approving FMV honoraria, securing venue, travel, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Plan and execute scientific/medical education (non-CME) such as: Scientific Symposia at congresses or web-based education, medical education content at congress booths, or other medical education activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engage internal and external subject matter experts, when appropriate, for participation in Medical Communications or Medical Education activities and content development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with the creation of other scientific documents (e.g., medical science liaison [MSL] training slide decks, training tools, and FAQs)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure Medical Communications initiatives and tactics are executed within agreed upon timeline and budget\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the commercial team on various tactics (e.g. Brand Plan and commercial materials)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree (i.e. PharmD, MD, PhD, RN, MS/MA) from an accredited university/program\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5+ years of experience of pharmaceutical industry experience, preferably in Medical Affairs, MSL, and/or Medical Communications experience in an agency or pharmaceutical environment with transferable skill set\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Pharmaceutical industry fellowship within Medical Affairs or Medical Communications may satisfy experience requirement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with cross-functional stakeholders and/or agencies to develop medical field materials/tools\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in liver disease or rare disease desired\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing vendors and budgets desired\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced computer and Internet skills, including knowledge of Word, PowerPoint, Excel, Veeva Systems, search engines (PubMed, etc.), references databases (e.g., EndNote, Reference Manager), etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with Microsoft PowerPoint is essential\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge and proficiency in Veeva Vault and Veeva CRM is strongly desired\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of regulations which guide promotional and non-promotional activities of pharmaceutical companies, and experience with their application\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent and effective interpersonal and communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be well-organized and able to multi-task in a fast-paced, deadline-driven environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to interact with internal stakeholders (i.e. commercial, clinical operations, statistics, regulatory, publications, etc.) and coordinate on appropriate scientific and medical activities as they relate to on-going medical affairs projects\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently with some supervision and guidance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel (US and International) approximately 25% of time\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $190,000 to $210,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033160007,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5157781007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4642239007,"location":{"name":"Foster City"},"metadata":null,"id":5157781007,"updated_at":"2026-06-06T11:18:18-04:00","requisition_id":"2026-REP-026","title":"Associate Director, Medical Communications (VLX)","company_name":"Mirum Pharmaceuticals","first_published":"2026-06-05T15:01:25-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director/Director, Medical Communications for the volixibat Portfolio Global Medical Affairs Team (GMAT) is a critical team role with a high-level of accountability, reporting to the GMAT Lead. This role will focus on developing and executing GMAT materials and initiatives, including development, approval, and roll-out of Field Medical Materials; creation of content for and execution of Medical Advisory Boards; and creation of content for and execution of Scientific Symposia and other Medical Education initiatives. The Associate Director/Director of Medical Communications will collaborate with external Medical Communications agencies and Medical Education partners to create timely, relevant, accurate, and engaging tools and programs that support Mirum scientific and medical objectives. They will also collaborate in the management of the database of Medical Field tools, including updating, archiving, and tracking of existing materials, and strategic planning and development of new tools based on the needs and objectives of the GMAT. Essential to this role is the ability to effectively communicate and work with internal stakeholders and external thought leaders in a fast-paced environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensuring Medical Affairs initiatives and tactics are executed within agreed upon timeline and budget\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organize scientific advisory boards and investigator meetings including operational planning for advisory boards (contracting with advisors, approving FMV honoraria, securing venue, travel, accommodations), content development and speaker preparation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Plan and execute congress related activities: session planning, KOL engagement, advocacy engagement, pre and post congress debriefs, daily debriefs, congress summary and educational and scientific booth activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Plan and execute scientific/medical education (non-CME) such as: scientific symposia at congresses, web-based medical education, along with the development of MSL materials (reactive and proactive)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working with/supporting the VLX GMAL on all medical affairs related activities,\u0026amp;nbsp;as well as with the Mirum leadership team (providing project tracker or status updates as needed)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supporting commercial on various tactics (e.g. Brand Plan and commercial materials)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s, Master’s, or Doctorate (i.e. RN, BS/BA, MS/MA, PharmD) level of degree from an accredited university/program\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5+ years of experience of pharmaceutical industry experience, preferably in Medical Affairs, MSL, and/or Medical Communications experience in an agency or pharmaceutical environment with transferable skill set\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possesses substantial understanding of liver disease or had rare disease experience.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced computer and Internet skills, including knowledge of Word, PowerPoint, Excel, Veeva Systems, search engines (PubMed, etc.), references databases (e.g., EndNote, Reference Manager), etc. Proficiency with Microsoft PowerPoint is essential.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to interact externally and internally to support global business strategy across assets and launches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must possess excellent oral and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to interact with and coordinates appropriate scientific and medical activities with internal stakeholders (i.e. commercial, clinical operations, statistics, regulatory, publications, chemistry, manufacturing, controls ‘CMC’ etc.) as they relate to on-going medical affairs projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represents or Mirum at external meetings including investigator meetings, scientific congresses, regulatory meetings, along with advisory boards etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently with some supervision and guidance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exercises sound judgment within well-defined practices and policies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage budget for assigned projects\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical experience/research background or knowledge in one of following areas: liver diseases, pediatrics/neonatal care, cholestasis or rare diseases is preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Environment:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;This is a high growth, fast paced organization. The ability to be productive and successful in a work environment is critical.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness and ability to travel domestically and internationally is required, it is anticipated that this will be 30% of work time.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $200,000 to $230,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033160007,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5156335007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4641514007,"location":{"name":"Charlotte, NC"},"metadata":null,"id":5156335007,"updated_at":"2026-06-04T18:55:35-04:00","requisition_id":"2026-REP-025","title":"Associate Director, Patient Services Operations","company_name":"Mirum Pharmaceuticals","first_published":"2026-06-04T18:49:48-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director, Patient Services Operations will manage the day-to-day hub operations for the Mirum in-house Mirum Access Plus (MAP) program, supporting Mirum’s product portfolio and continued expansion over time. The Associate Director will support the Director, Patient Services Operations, leading all day-to-day operations of their team. Duties will include overseeing ensuring all KPIs are met or exceeded, anticipating/identifying/resolving potential operational challenges, overseeing accurate and timely reporting of results, monitoring program budgets, and ensuring all legal, regulatory and pharmacovigilance requirements are being met. The Associate Director will also interact regularly with brand teams and other internal functional areas including finance, legal, safety, quality, training and others as needed.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Team Leadership: \u0026lt;/strong\u0026gt;Lead a team responsible for specialty pharmacy access, reimbursement, and affordability activities. This includes, but not limited to supporting day-to-day activities, managing work queues, delegating assignments, developing team skills, establishing baseline goals, and motivating the team. Develop plans for team members within the team to support in achieving their desired goals. Ensure team goals are aligned with overall organizational strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Program Operations: \u0026lt;/strong\u0026gt;Ensure that all program operations are running smoothly and in accordance with program business rules and all safety, legal and regulatory requirement. Collaborate with Mirum internal stakeholders and partner vendors to update business rules as appropriate. Work with internal MAP team to track and meet or exceed all program KPIs including call volumes, wait times, benefits investigation turnaround times.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Vendor Management\u0026lt;/strong\u0026gt;: Serve as liaison between Mirum and MAP service vendors. Anticipate and address program challenges and adapt business processes to improve the MAP program.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Reporting\u0026lt;/strong\u0026gt;: Work with Mirum’s Commercial Insights \u0026amp;amp; Analytics (CIA) to ensure that all key MAP data is reported on time and accurately through the data feeds. Develop and distribute summary reports to key Mirum colleagues on a regular basis. Work with CIA to prepare ad hoc reports as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Pharmacovigilance (PV)\u0026lt;/strong\u0026gt;: Collaborate with PV vendor and Mirum drug safety team to ensure that all adverse events (AEs) and product complaints are reported at the right time in accordance with Mirum guidelines. Serve as point person for Safety team for any data requests related to AEs or to help coordinate required audits of the MAP program.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Co-pay Program\u0026lt;/strong\u0026gt;: Oversee operations for co-pay program for Mirum products. Manage the MAP team co-pay card enrollment process through the copay vendor integration and/or established process. Develop and update co-pay program terms and conditions for patient notification. Serve as key liaison with co-pay program vendor. Ensure timely reporting of key co-pay program data, and that all co-pay program KPIs are met or exceeded. Collaborate with brand team to develop co-pay program offers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Budgeting\u0026lt;/strong\u0026gt;: Support Director, Patient Services Operations with developing, maintaining and meeting all program budget requirements. Assist with forecasting. provide Director with timely alerts regarding potential budget overages.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Patient Access Support (PAS)/Field Reimbursement Managers:\u0026lt;/strong\u0026gt; Support Senior Director, US Payer Account Lead with maintaining open lines of communication between PAS team and MAP team as appropriate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Director, Patient Services Operations on new program launches. Assist with RFPs as required. Provide input to strategic planning for new MAP offerings and developing key requirements for new programs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BA/BS degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;7+ years of experience in the pharmaceutical/biotech industry, or experience with a Hub service provider or in-house hub.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with pharmacy benefits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated depth with reimbursement support services and hubs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of legal/regulatory/safety requirements with hubs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with patient assistance (free medicine) programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of coding associated with claims reimbursement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work cross-functionally as need to achieve desired results.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to advance and complete projects on time and within budget.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Anticipate and address challenges to ensure smooth operations of hub services.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to solve problems quickly and efficiently in a collaborative manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal and communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong business acumen.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4054753007,"name":"Charlotte","location":"North Carolina, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5108432007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4618367007,"location":{"name":"Foster City"},"metadata":null,"id":5108432007,"updated_at":"2026-06-01T19:37:16-04:00","requisition_id":"2026-MAY-004","title":"Associate Director, Program Management","company_name":"Mirum Pharmaceuticals","first_published":"2026-04-14T18:46:11-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director, Program Management plays a central role within Mirum by providing program management expertise and ensuring cross-functional planning and execution. The program manager partners with the Program Lead and functional leads to develop and manage the integrated product plan, develop timelines, and ensure adherence to the budget for one of our pipeline programs.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support the Program Lead with the development, communication, and timely execution of the program strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organize and drive effective and action-oriented program team meetings by preparing and distributing agendas/minutes, identifying and tracking decisions and action items to resolution, and escalating areas of concern as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with the Program Lead to facilitate effective cross-functional decision making with transparent communication and clear escalation pathways\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate identification of risks which could impact the program’s strategic goals; propose and implement plans to mitigate risks or develop contingencies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain integrated program timelines in conjunction with functional leads\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and communicate program priorities, interdependencies, and critical path activities to all stakeholders to allow long term planning, including resource allocation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organize the preparation of high-quality documents for review by governance committees in collaboration with the Program Lead and program team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepares and provides project documents and information for monthly reports, executive team updates, and board meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Program Lead and finance and accounting to develop annual operating plan components related to assigned program and support budget management by timely identification of out-of-scope activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate and manage special program-related projects, as assigned\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the standardization of project management best practices at Mirum\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelors Degree or higher in scientific/healthcare/business field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience (7+ years) in clinical research and project management within the pharmaceutical industry (Biotech/small pharma experience preferred).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in rare disease and/or liver disease is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong ability to communicate effectively with team members creating an environment that fosters successful teamwork, collaboration and cooperation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thorough understanding of clinical trial management processes and the operation of all clinical development functional areas.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to prepare timelines and present related information to management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to identify risks, propose mitigation strategies, and remove barriers to success.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail and the ability to work collaboratively with Project Lead to establish priorities for team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise in developing and managing project scope, deliverables, risks and resource requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of project management software packages and the Microsoft Office Suite: Excel, Project, PowerPoint, Word and Outlook; ability to create effective presentations for internal and external use.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in a fast paced environment with demonstrated ability to juggle multiple competing tasks and demands, across time-zones, while maintaining positive attitude.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently, take initiative, complete tasks to deadlines and support product team in doing the same.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and oral communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Displays a high level of professionalism with internal and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of current regulatory requirements and guidelines governing clinical research. (e.g. ICH/GCP).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $195,084 to $225,217 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033162007,"name":"R\u0026D","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5119672007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4623714007,"location":{"name":"Foster City"},"metadata":null,"id":5119672007,"updated_at":"2026-06-01T19:41:30-04:00","requisition_id":"2026-MAY-020","title":"Associate Director, Quality System, QMS","company_name":"Mirum Pharmaceuticals","first_published":"2026-04-27T09:30:49-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Leads roll out and oversight of Veeva QMS modules, ensuring compliance with applicable regulatory requirements. Manages the development, implementation, and continuous improvement of policies and procedures to maintain quality standards aligned with global regulatory and company guidelines. Partners cross-functionally to ensure effective execution of quality processes. Applies strong knowledge of global regulations to support compliant and efficient operations. Contributes to the strategic direction and ongoing performance of the Quality Management System (QMS), driving consistency, inspection readiness, and continuous improvement initiatives.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the end-to-end implementation and rollout of new modules within Veeva, ensuring alignment with business needs and regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the Quality Systems lead and subject matter expert (SME) processes, driving standardization and harmonization across the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with cross-functional stakeholders (Quality Assurance, Manufacturing, Supply Chain, and IT) to define system requirements, workflows, and business processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee system configuration, user acceptance testing (UAT), and validation activities (e.g., CSV/CSA) to ensure the system is fit for intended use and compliant with global GMP regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with developing and executing implementation plans, including timelines, resource planning, risk mitigation strategies, and communication plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and/or review governing documents (SOPs, work instructions, and training materials) to support the new modules and ensure alignment with QMS requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead training strategy and rollout, including role-based curricula, to ensure successful user adoption and adherence to new processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor system performance and user feedback post-implementation; identify and implement continuous improvements and enhancements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with internal stakeholders to ensure alignment and effective utilization of newly implemented and current modules.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as the primary point of contact for system-related issues, deviations, and change controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support internal and external audits and health authority inspections by providing system documentation, demonstrating functionality, and addressing inquiries.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in scientific discipline\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;12+ years’ experience and strong background in Quality and Quality Systems in the drug development industry with knowledge of cGMP/ICH/FDA/EMA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience implementing or supporting electronic QMS platforms, ideally Veeva Vault QMS\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management and change management skills is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to drive process standardization and continuous improvement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate a quality mindset and ability to influence across the organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Successful experience writing and reviewing SOPs and other Quality documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expert knowledge of phase appropriate cGxPs and experience leading Quality System implementation and continuous improvement efforts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to successfully interact with regulatory health authorities at inspections and thorough understanding of audit and vendor management programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational skills: Proactive, management of multiple tasks of varying complexity simultaneously\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills including relationship building, conflict resolution, and verbal and written communication are essential in this collaborative work environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $190,000 to $205,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033155007,"name":"Quality Assurance","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5147766007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4637318007,"location":{"name":"Foster City"},"metadata":null,"id":5147766007,"updated_at":"2026-06-01T19:43:18-04:00","requisition_id":"2026-MAY-016","title":"Associate Director, Regulatory Affairs Advertising and Promotion","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-27T13:59:20-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director, Regulatory Affairs Advertising and Promotion provides regulatory guidance on commercial regulatory activities to enable the business to meet its commercial needs in a compliant manner. This position will provide regulatory guidance as a member of the Medical, Legal and Regulatory (MLR). This role is accountable for helping develop strategies and timelines, and managing internal team discussions to support preparation of advertising and promotional materials for regulatory submissions. This role will report to the Director, Global Regulatory Affairs Advertising and Promotion.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Responsible for providing commercial regulatory oversight for assigned programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage and author commercial regulatory submissions, working closely with the Publishing vendor to ensure timely publishing and submission of promotional materials to the Office of Prescription Drug Promotion (OPDP).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide regulatory guidance on new concepts and new campaigns.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain a continued awareness and understanding of FDA regulations, guidance documents, and enforcement actions with regards to advertising and promotion of pharmaceutical products. Help monitor enforcement trends and provide timely advice to the team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Recognized as a resource for commercial regulatory advice across departments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;May contribute to process improvements relevant to commercial regulatory activities, including the MLR Committee.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Aid in the development and implementation of regulatory advertising and promotional processes, as necessary.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s or advanced degree in a scientific discipline, with a minimum of 8 years in Regulatory Affairs with a minimum of 6 years of experience in the regulatory review of advertising and promotional materials for prescription drug and/or biologic products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience representing Commercial Regulatory Affairs on cross functional teams is desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent planning and organizational skills and the ability to work simultaneously on multiple projects with tight timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication skills both in writing and verbally.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with FDA’s Office of Prescription Drug Promotion (OPDP) submissions and strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth knowledge of regulatory requirements associated with advertising and promotion of prescription drug products is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of and experience with laws and regulations regarding marketing pharmaceuticals in rest of world (ROW) is highly desired.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal, written, negotiation, influence and interpersonal communication skills are required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capable of critically reviewing complex technical/scientific documents and influencing colleagues across functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Requires ability to work both independently and in a team environment, to set priorities to meet timelines, to influence others.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to engage multiple stakeholders to achieve the business objective.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organized with systematic approach to prioritization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Process oriented to achieve the business objective.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Environment:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;This is a high growth, fast paced organization. The ability to be productive and successful in a work environment is critical.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Some travel required. Responsibilities may require a work schedule that may include working outside of “normal” work hours, to meet business demands of a global company.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $205,000 to $225,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033161007,"name":"Regulatory Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5145618007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4636271007,"location":{"name":"US Remote"},"metadata":null,"id":5145618007,"updated_at":"2026-06-02T17:59:41-04:00","requisition_id":"2026-MAY-023","title":"Associate Director, Strategic Engagement (Thought Leader Liaison), Central","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-27T18:22:16-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate\u0026amp;nbsp;Director, Strategic Engagement also known as Thought Leader Liaison (TLL) serves as a key strategic partner between Mirum Pharmaceuticals and the healthcare community, focusing on cultivating and maintaining relationships with key opinion leaders (KOLs), thought leaders, and other external stakeholders. This role is responsible for building scientific credibility, supporting brand strategy, and ensuring aligned, compliant engagement with external experts to enhance awareness and education.\u0026amp;nbsp; Area of focus will largely be supporting the Hepatology and Gastroenterology community supporting our existing and future products in Alagille, PFIC, PBC, PSC and Hepatitis D.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;States likely to be included in territory include: \u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;TX, OK, CO, UT, KS, NE, MN\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and communicate the strategic vision and operational plan for engaging KOLs.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and oversee development and execution of individual KOL Mapping KOLs plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with the Director, Marketing – KOL Strategy and Congress Planning to ensure alignment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain productive, collaborative, and compliant relationships with peers leading teams in Marketing, Market Access, Patient Services, and Medical Affairs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with the Field Sales team on the execution of all thought leader-related initiatives and programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build mechanisms to collect insights, synthesize and integrate them, and communicate to brand to inform tactics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bring thought leaders closer to Mirum by ensuring compliant, value-added connections across the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Medical Leadership on engagement strategy and planning as appropriate, including support and coordination of commercial advisory boards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engage with KOLs to solicit feedback that shapes and informs brand strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute Marketing strategy for conferences/congresses including sponsorships, communication/messaging, and advocacy group engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work in partnership with the Marketing portfolio leaders and field leadership to develop appropriate KPIs and metrics to support the brand marketing and executional goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as primary point of contact for the field, maintaining an effective two-way dialogue on KOL engagement, potential speaker identification, and up-and-coming thought leaders and experts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze market data, confirm data reliability and inform team stakeholders to make informed decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively engage partners in Legal and Compliance to ensure programs and processes are being delivered with the highest ethical standards\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree (required)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 10 years of pharmaceutical or related industry experience required, mostly\u0026amp;nbsp;in a customer-facing capacity\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 3 years of working with Hepatology KOLs preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 2 years of working as a Thought Leader Liaison preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strategic thinking and an ability to work in a hands-on manner to deliver on multiple priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to draw insights from a variety of sources, understands market and competition.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Compiles relevant data from appropriate sources and performs analysis.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working successfully within a cross collaborative internal environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Synthesize complex and diverse information, recognizes trends and/or interrelationship.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to meet objectives and deadlines, promote efficiency and effectiveness, and incorporate improvements and program return on investment (ROI).\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management experience and the ability to manage and coordinate projects with multiple internal stakeholders and vendors on time\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal, written, organization and interpersonal skills required.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Versed in MS Office tools including Word, PowerPoint, and Outlook.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Approximately 65% domestic travel throughout the US. \u0026amp;nbsp;Selected candidate must live near a major airport and be able to travel regularly throughout the assigned area and attend meetings at both Mirum office and off-site locations through the US.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;#LI-REMOTE\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4032948007,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5145629007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4636279007,"location":{"name":"US Remote"},"metadata":null,"id":5145629007,"updated_at":"2026-06-02T18:01:34-04:00","requisition_id":"2026-MAY-024","title":"Associate Director, Strategic Engagement (Thought Leader Liaison),  Mid-Atlantic","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-27T18:24:12-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate\u0026amp;nbsp;Director, Strategic Engagement also known as Thought Leader Liaison (TLL) serves as a key strategic partner between Mirum Pharmaceuticals and the healthcare community, focusing on cultivating and maintaining relationships with key opinion leaders (KOLs), thought leaders, and other external stakeholders. This role is responsible for building scientific credibility, supporting brand strategy, and ensuring aligned, compliant engagement with external experts to enhance awareness and education.\u0026amp;nbsp; Area of focus will largely be supporting the Hepatology and Gastroenterology community supporting our existing and future products in Alagille, PFIC, PBC, PSC and Hepatitis D.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;States likely to be included in territory include: \u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;PA, DE, VA, MD, DC, WV, OH, KY\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and communicate the strategic vision and operational plan for engaging KOLs.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and oversee development and execution of individual KOL Mapping KOLs plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with the Director, Marketing – KOL Strategy and Congress Planning to ensure alignment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain productive, collaborative, and compliant relationships with peers leading teams in Marketing, Market Access, Patient Services, and Medical Affairs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with the Field Sales team on the execution of all thought leader-related initiatives and programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build mechanisms to collect insights, synthesize and integrate them, and communicate to brand to inform tactics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bring thought leaders closer to Mirum by ensuring compliant, value-added connections across the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Medical Leadership on engagement strategy and planning as appropriate, including support and coordination of commercial advisory boards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engage with KOLs to solicit feedback that shapes and informs brand strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute Marketing strategy for conferences/congresses including sponsorships, communication/messaging, and advocacy group engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work in partnership with the Marketing portfolio leaders and field leadership to develop appropriate KPIs and metrics to support the brand marketing and executional goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as primary point of contact for the field, maintaining an effective two-way dialogue on KOL engagement, potential speaker identification, and up-and-coming thought leaders and experts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze market data, confirm data reliability and inform team stakeholders to make informed decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively engage partners in Legal and Compliance to ensure programs and processes are being delivered with the highest ethical standards\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree (required)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 10 years of pharmaceutical or related industry experience required, mostly\u0026amp;nbsp;in a customer-facing capacity\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 3 years of working with Hepatology KOLs preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 2 years of working as a Thought Leader Liaison preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strategic thinking and an ability to work in a hands-on manner to deliver on multiple priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to draw insights from a variety of sources, understands market and competition.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Compiles relevant data from appropriate sources and performs analysis.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working successfully within a cross collaborative internal environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Synthesize complex and diverse information, recognizes trends and/or interrelationship.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to meet objectives and deadlines, promote efficiency and effectiveness, and incorporate improvements and program return on investment (ROI).\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management experience and the ability to manage and coordinate projects with multiple internal stakeholders and vendors on time\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal, written, organization and interpersonal skills required.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Versed in MS Office tools including Word, PowerPoint, and Outlook.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Approximately 65% domestic travel throughout the US. \u0026amp;nbsp;Selected candidate must live near a major airport and be able to travel regularly throughout the assigned area and attend meetings at both Mirum office and off-site locations through the US.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;#LI-REMOTE\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4032948007,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5145647007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4636287007,"location":{"name":"US Remote"},"metadata":null,"id":5145647007,"updated_at":"2026-06-02T18:04:08-04:00","requisition_id":"2026-MAY-033","title":"Associate Director, Strategic Engagement (Thought Leader Liaison), Midwest","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-27T18:25:59-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate\u0026amp;nbsp;Director, Strategic Engagement also known as Thought Leader Liaison (TLL) serves as a key strategic partner between Mirum Pharmaceuticals and the healthcare community, focusing on cultivating and maintaining relationships with key opinion leaders (KOLs), thought leaders, and other external stakeholders. This role is responsible for building scientific credibility, supporting brand strategy, and ensuring aligned, compliant engagement with external experts to enhance awareness and education.\u0026amp;nbsp; Area of focus will largely be supporting the Hepatology and Gastroenterology community supporting our existing and future products in Alagille, PFIC, PBC, PSC and Hepatitis D.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;States likely to be included in territory include: \u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;MI, IN, IL, WI, IA, MO\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and communicate the strategic vision and operational plan for engaging KOLs.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and oversee development and execution of individual KOL Mapping KOLs plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with the Director, Marketing – KOL Strategy and Congress Planning to ensure alignment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain productive, collaborative, and compliant relationships with peers leading teams in Marketing, Market Access, Patient Services, and Medical Affairs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with the Field Sales team on the execution of all thought leader-related initiatives and programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build mechanisms to collect insights, synthesize and integrate them, and communicate to brand to inform tactics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bring thought leaders closer to Mirum by ensuring compliant, value-added connections across the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Medical Leadership on engagement strategy and planning as appropriate, including support and coordination of commercial advisory boards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engage with KOLs to solicit feedback that shapes and informs brand strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute Marketing strategy for conferences/congresses including sponsorships, communication/messaging, and advocacy group engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work in partnership with the Marketing portfolio leaders and field leadership to develop appropriate KPIs and metrics to support the brand marketing and executional goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as primary point of contact for the field, maintaining an effective two-way dialogue on KOL engagement, potential speaker identification, and up-and-coming thought leaders and experts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze market data, confirm data reliability and inform team stakeholders to make informed decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively engage partners in Legal and Compliance to ensure programs and processes are being delivered with the highest ethical standards\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree (required)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 10 years of pharmaceutical or related industry experience required, mostly\u0026amp;nbsp;in a customer-facing capacity\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 3 years of working with Hepatology KOLs preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 2 years of working as a Thought Leader Liaison preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strategic thinking and an ability to work in a hands-on manner to deliver on multiple priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to draw insights from a variety of sources, understands market and competition.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Compiles relevant data from appropriate sources and performs analysis.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working successfully within a cross collaborative internal environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Synthesize complex and diverse information, recognizes trends and/or interrelationship.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to meet objectives and deadlines, promote efficiency and effectiveness, and incorporate improvements and program return on investment (ROI).\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management experience and the ability to manage and coordinate projects with multiple internal stakeholders and vendors on time\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal, written, organization and interpersonal skills required.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Versed in MS Office tools including Word, PowerPoint, and Outlook.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Approximately 65% domestic travel throughout the US. \u0026amp;nbsp;Selected candidate must live near a major airport and be able to travel regularly throughout the assigned area and attend meetings at both Mirum office and off-site locations through the US.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;#LI-REMOTE\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4032948007,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5148241007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4637562007,"location":{"name":"US Remote"},"metadata":null,"id":5148241007,"updated_at":"2026-06-02T18:06:16-04:00","requisition_id":"2026-REP-023","title":"Associate Director, Strategic Engagement (Thought Leader Liaison), Northeast","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-27T18:30:02-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate\u0026amp;nbsp;Director, Strategic Engagement also known as Thought Leader Liaison (TLL) serves as a key strategic partner between Mirum Pharmaceuticals and the healthcare community, focusing on cultivating and maintaining relationships with key opinion leaders (KOLs), thought leaders, and other external stakeholders. This role is responsible for building scientific credibility, supporting brand strategy, and ensuring aligned, compliant engagement with external experts to enhance awareness and education.\u0026amp;nbsp; Area of focus will largely be supporting the Hepatology and Gastroenterology community supporting our existing and future products in Alagille, PFIC, PBC, PSC and Hepatitis D.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;States likely to be included in territory include: \u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;NY, NJ, CT, MA, RI, VT, NH, ME\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and communicate the strategic vision and operational plan for engaging KOLs.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and oversee development and execution of individual KOL Mapping KOLs plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with the Director, Marketing – KOL Strategy and Congress Planning to ensure alignment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain productive, collaborative, and compliant relationships with peers leading teams in Marketing, Market Access, Patient Services, and Medical Affairs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with the Field Sales team on the execution of all thought leader-related initiatives and programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build mechanisms to collect insights, synthesize and integrate them, and communicate to brand to inform tactics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bring thought leaders closer to Mirum by ensuring compliant, value-added connections across the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Medical Leadership on engagement strategy and planning as appropriate, including support and coordination of commercial advisory boards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engage with KOLs to solicit feedback that shapes and informs brand strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute Marketing strategy for conferences/congresses including sponsorships, communication/messaging, and advocacy group engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work in partnership with the Marketing portfolio leaders and field leadership to develop appropriate KPIs and metrics to support the brand marketing and executional goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as primary point of contact for the field, maintaining an effective two-way dialogue on KOL engagement, potential speaker identification, and up-and-coming thought leaders and experts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze market data, confirm data reliability and inform team stakeholders to make informed decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively engage partners in Legal and Compliance to ensure programs and processes are being delivered with the highest ethical standards\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree (required)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 10 years of pharmaceutical or related industry experience required, mostly\u0026amp;nbsp;in a customer-facing capacity\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 3 years of working with Hepatology KOLs preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 2 years of working as a Thought Leader Liaison preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strategic thinking and an ability to work in a hands-on manner to deliver on multiple priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to draw insights from a variety of sources, understands market and competition.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Compiles relevant data from appropriate sources and performs analysis.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working successfully within a cross collaborative internal environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Synthesize complex and diverse information, recognizes trends and/or interrelationship.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to meet objectives and deadlines, promote efficiency and effectiveness, and incorporate improvements and program return on investment (ROI).\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management experience and the ability to manage and coordinate projects with multiple internal stakeholders and vendors on time\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal, written, organization and interpersonal skills required.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Versed in MS Office tools including Word, PowerPoint, and Outlook.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Approximately 65% domestic travel throughout the US. \u0026amp;nbsp;Selected candidate must live near a major airport and be able to travel regularly throughout the assigned area and attend meetings at both Mirum office and off-site locations through the US.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;#LI-REMOTE\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4032948007,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5148247007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4637565007,"location":{"name":"US Remote"},"metadata":null,"id":5148247007,"updated_at":"2026-06-02T18:08:03-04:00","requisition_id":"2026-MAY-032","title":"Associate Director, Strategic Engagement (Thought Leader Liaison), West","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-27T18:31:31-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate\u0026amp;nbsp;Director, Strategic Engagement also known as Thought Leader Liaison (TLL) serves as a key strategic partner between Mirum Pharmaceuticals and the healthcare community, focusing on cultivating and maintaining relationships with key opinion leaders (KOLs), thought leaders, and other external stakeholders. This role is responsible for building scientific credibility, supporting brand strategy, and ensuring aligned, compliant engagement with external experts to enhance awareness and education.\u0026amp;nbsp; Area of focus will largely be supporting the Hepatology and Gastroenterology community supporting our existing and future products in Alagille, PFIC, PBC, PSC and Hepatitis D.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;States likely to be included in territory include: CA, AZ, NV, OR, WA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and communicate the strategic vision and operational plan for engaging KOLs.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and oversee development and execution of individual KOL Mapping KOLs plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with the Director, Marketing – KOL Strategy and Congress Planning to ensure alignment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain productive, collaborative, and compliant relationships with peers leading teams in Marketing, Market Access, Patient Services, and Medical Affairs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with the Field Sales team on the execution of all thought leader-related initiatives and programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build mechanisms to collect insights, synthesize and integrate them, and communicate to brand to inform tactics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bring thought leaders closer to Mirum by ensuring compliant, value-added connections across the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Medical Leadership on engagement strategy and planning as appropriate, including support and coordination of commercial advisory boards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engage with KOLs to solicit feedback that shapes and informs brand strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute Marketing strategy for conferences/congresses including sponsorships, communication/messaging, and advocacy group engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work in partnership with the Marketing portfolio leaders and field leadership to develop appropriate KPIs and metrics to support the brand marketing and executional goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as primary point of contact for the field, maintaining an effective two-way dialogue on KOL engagement, potential speaker identification, and up-and-coming thought leaders and experts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze market data, confirm data reliability and inform team stakeholders to make informed decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively engage partners in Legal and Compliance to ensure programs and processes are being delivered with the highest ethical standards\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree (required)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 10 years of pharmaceutical or related industry experience required, mostly\u0026amp;nbsp;in a customer-facing capacity\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 3 years of working with Hepatology KOLs preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 2 years of working as a Thought Leader Liaison preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strategic thinking and an ability to work in a hands-on manner to deliver on multiple priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to draw insights from a variety of sources, understands market and competition.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Compiles relevant data from appropriate sources and performs analysis.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working successfully within a cross collaborative internal environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Synthesize complex and diverse information, recognizes trends and/or interrelationship.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to meet objectives and deadlines, promote efficiency and effectiveness, and incorporate improvements and program return on investment (ROI).\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management experience and the ability to manage and coordinate projects with multiple internal stakeholders and vendors on time\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal, written, organization and interpersonal skills required.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Versed in MS Office tools including Word, PowerPoint, and Outlook.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Approximately 65% domestic travel throughout the US. \u0026amp;nbsp;Selected candidate must live near a major airport and be able to travel regularly throughout the assigned area and attend meetings at both Mirum office and off-site locations through the US.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;#LI-REMOTE\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4032948007,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5079006007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4605024007,"location":{"name":"Foster City"},"metadata":null,"id":5079006007,"updated_at":"2026-06-02T19:07:20-04:00","requisition_id":"2026-INC-011","title":"Director, Clinical Development","company_name":"Mirum Pharmaceuticals","first_published":"2026-03-13T14:40:00-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director/Senior Director, Clinical Development will be responsible for all clinical trial related activities for Brelovitug, a key asset in Phase 3 on a cross-functional team of internal and external experts, investigators and government agencies. Activities include but are not limited to protocol development, support study startup, oversight of trial execution, recruitment, ongoing clinical development management and closeout as appropriate. Compliance with internal processes, GCP/ICH and regulatory requirements, study and data monitoring, data analysis are required. Participation in health authority meetings and regulatory filing activities are also part of this role. The Director/Senior Director, Clinical Development operates in collaboration with other functions including internal Safety, Regulatory, Biometrics, and Clinical Operations teams.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Leadership and management of all aspects of complex, global development clinical studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Primary point of contact for clinical inquiries from sites, CRO and site monitors; answer or triage questions as appropriate integration of clinical/regulatory strategy into global product development strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Primary liaison for internal Clinical Operations for site selection, site start-up activities, study management and closeout activities, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the creation of and/or review of clinical slides for internal and external meetings (e.g. Investigator Meetings, SIVs, IDMCs, Advisory Boards, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in authoring key clinical study documents, including Protocols, Clinical Study Reports, Investigator Brochures, Regulatory Authority briefing books, Development Safety Update Reports etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic input on the overall development plan, internal and external evaluation of new studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversight of clinical aspects of compliance of and inspection readiness in completed, ongoing and starting clinical trials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaboration in the analysis and writing of scientific publications/presentations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Works closely with cross-functional team members\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Co-leads Study Management Team with Clinical Operations lead.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;MD, PharmD, PhD or equivalent is preferred with ≥3 years of drug development in industry, academia, or a related environment, working within cross‑functional project or program teams with proven success.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in Liver or rare disease a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge and understanding of regulatory requirements for product approval and compliance in US and Europe.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated accountability for delivery on clinical studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leadership in clinical development programs and multidisciplinary trial teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with basic statistical principles and techniques of data analysis, interpretation and clinical relevance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to understand and communicate risks, as well as develop and execute contingency plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to think creatively and develop and execute in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail oriented with exceptional organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective communicator with strong verbal and written skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to identify issues, analyze situations and provide effective solutions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of the clinical development process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of applicable regulatory.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Environment:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;This is a high growth, fast paced organization. The ability to be productive and successful in a work environment is critical.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness and ability to travel domestically and internationally is required, it is anticipated that this will be 20% of work time.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $220,000 to $240,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033162007,"name":"R\u0026D","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5147852007","data_compliance":[{"type":"gdpr","requires_consent":true,"requires_processing_consent":true,"requires_retention_consent":true,"retention_period":365,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4637362007,"location":{"name":"Basel"},"metadata":null,"id":5147852007,"updated_at":"2026-05-27T15:12:21-04:00","requisition_id":"2026-MAY-001","title":"Director, Global Regulatory Affairs ","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-27T15:12:21-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director, Global Regulatory Affairs – International Region will play a significant role in providing International (ex‑North America) regulatory strategic leadership and execution for assigned clinical development and lifecycle management programs associated with rare diseases. This role will represent the regulatory function and provide guidance across internal R\u0026amp;amp;D stakeholders and cross‑functional Program Teams, including Clinical Development, Clinical Operations, Biometrics, Nonclinical, Pharmacovigilance, Quality, Regulatory CMC, Regulatory Labelling, Regulatory Project Management, Medical Writing, corporate partners, and distributors, as applicable, across multiple countries.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director will act as the Regional Regulatory Lead for assigned projects and support Global Regulatory Project Team activities, ensuring International regulatory compliance and the timely delivery of submissions, approvals, and lifecycle management procedures. The scope includes, but is not limited to, high-quality regulatory submissions of original applications (i.e., NDAs, MAAs, INDs, etc.), clinical trial applications, rare disease designations, major supplements/variations, and lifecycle submissions for assigned programs in International markets, as applicable.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Regulatory Strategy and Leadership\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and lead International regulatory strategies for assigned programs in alignment with global development and commercial objectives, under the guidance of senior Global Regulatory Affairs leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the Regional Regulatory Lead for assigned programs and represent International Regulatory Affairs on Program Teams and Global Regulatory Project Teams, as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide International regulatory guidance across the product lifecycle, including development strategy, country and regional requirements, submission planning, change control assessment, registration pathways, and lifecycle management.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Cross-functional Planning and Execution\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Contribute to Global Regulatory Project Team meetings in partnership with the Global Regulatory Lead and Regulatory Project Management, ensuring clear plans, timelines, risks, assumptions, decision points, and cross-functional alignment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and/or oversee the preparation of regulatory documentation for Health Authority interactions, including meeting requests, briefing packages, clinical trial applications, marketing authorization applications, variations and amendments, and responses to Health Authority questions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Critically review submission documents to ensure scientific quality, regulatory compliance, consistency, and alignment with agreed International and global regulatory strategy.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Stakeholder Collaboration and External Engagement\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with Regulatory Project Management, Regulatory CMC, Regulatory Labelling, Medical Writing, Clinical Operations, Clinical Development, Nonclinical, Pharmacovigilance, Quality, Biometrics, Commercial, and other cross-functional stakeholders to deliver timely, high-quality International regulatory outputs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain effective relationships with international partners, distributors, local regulatory representatives, and external vendors to support submissions, approvals, and post-approval activities across International markets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in Health Authority meetings and support preparation, negotiation strategy, meeting conduct, follow-up actions, and communication of outcomes to internal stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Regulatory Operations and Compliance\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Contribute to and review responses to Health Authority questions to ensure they are appropriate, consistent, complete, and strategically aligned across International markets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain current knowledge of EMA, EU, UK, Swiss, and other International regulatory requirements, guidance, and industry practices, while remaining aware of US FDA and Health Canada requirements that may affect global development strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support major regulatory procedures and deliverables, including MAA-related activities, clinical trial applications, Pediatric Investigation Plans, Orphan Drug Designation activities, post-marketing commitments, variations and amendments, and lifecycle management activities, as applicable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with technical, medical writing, and cross-functional colleagues to support International product prioritization and special designation requests, where applicable, and ensure alignment with broader development strategy.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Communication and Team Support\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Clearly articulate regulatory challenges, risks, options, and potential solutions, and make practical recommendations to Global Regulatory Project Teams, Program Teams, International leadership, and senior management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage direct report(s), if applicable, and provide mentorship, coaching, and functional guidance to junior regulatory professionals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the Senior Director, Global Regulatory Affairs, and International Leadership Team activities, as required.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Academic Background\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in biological or life sciences, pharmacy, medicine, or a related scientific discipline, or an international equivalent.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An advanced degree is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Industry and Regulatory Experience\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;10+ years of experience in the pharmaceutical industry, including 8–10 years in Global Regulatory Affairs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of drug development and substantial experience with international regulatory procedures and major Health Authorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience developing and executing regulatory strategies for clinical development programs and marketed products, ideally in rare disease or specialty therapeutics.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Regulatory Scope and Submissions\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of EMA, EU, UK, Swiss, and broader international regulatory guidance, regulations, drug development processes, and industry practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of US FDA and Health Canada requirements is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with major regulatory submissions and procedures—including clinical trial applications, MAAs, NDA/NDS support, Pediatric Investigation Plans, Orphan Drug Designation activities, variations and amendments, post-approval commitments, and lifecycle management activities—is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Strategic Leadership\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience in strategic problem-solving, Health Authority negotiations, and leading cross-functional teams on product regulatory strategy.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Communication and Judgement\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ability to understand, synthesize, and communicate complex scientific and regulatory information clearly to support regulatory strategy and submissions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills, with strong personal integrity and sound judgment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to clearly articulate regulatory challenges, identify potential solutions, and recommend pragmatic paths forward in emails, presentations, and team discussions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Strategic and Regulatory Leadership\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong strategic problem-solving, negotiation, and decision-making skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead decision-making within cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently, escalate key issues appropriately, influence senior stakeholders, set strategic direction, and navigate ambiguity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience across multiple phases of clinical development, including late-stage development and post-marketing activities, is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Collaboration and Influence\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ability to build effective working relationships with internal stakeholders, Health Authorities, partners, distributors, local regulatory representatives, and external vendors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated organizational awareness, including experience working cross-functionally, influencing without authority, and representing Regulatory Affairs on global teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive, collaborative, and solution-oriented, with strong organizational discipline.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Execution and People Leadership\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Excellent planning and organizational skills, with the ability to manage multiple projects, priorities, and tight timelines in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;People management or mentoring experience is preferred, with the ability to provide clear direction, coaching, and feedback to team members.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;WORK ENVIRONMENT\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;This is a high‑growth, fast‑paced organization. The ability to be productive, collaborative, and team‑oriented is critical.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness and ability to travel domestically and internationally is required; anticipated travel is approximately 10–15% of work time.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;On‑site presence at the Basel office is required, with a minimum of 2 days per week unless otherwise agreed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033161007,"name":"Regulatory Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4033153007,"name":"Basel","location":"Basel, Basel-Stadt, Switzerland","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5126677007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4627060007,"location":{"name":"Foster City"},"metadata":null,"id":5126677007,"updated_at":"2026-06-02T19:24:17-04:00","requisition_id":"2026-FEB-005","title":"Director, Medical Writing","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-01T15:10:03-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Director, Medical Writing works closely with stakeholders in Clinical Development, Clinical Operations, Biostatistics, and other functional areas and manages medical writing service providers to develop Regulatory documents, including but not limited to clinical study protocols and clinical protocol amendments, clinical study reports, patient narratives, clinical development plans, IND submissions, integrated summary reports, NDA/MAA and eCTD submissions, and Investigator Brochures, etc.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Participate in and oversee vendors for the writing, editing, and confirmation of the scientific and medical accuracy of clinical and regulatory documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work collaboratively to incorporate/adjudicate comments from internal and external stakeholders through document development to produce final high-quality deliverables.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact with internal stakeholders and with external service providers to ensure the timely development, review, and publication of documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Critically analyze complex data and information and collaborate with clinical, medical, and biostatistics/data science teams on data analysis, description, and presentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate the development of the documents named above and others as assigned by the Head of Medical Writing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure quality control of documents as well as formatting finalization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide support in development of submission-level documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure adherence to timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist the Head of Medical Writing in coordinating workload and maintaining a high standard. Effectively manage multiple assignments in parallel.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare documents in accordance with Mirum SOP and specifications as applicable, and relevant ICH and regulatory/industry guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review of Statistical Analysis Plan (SAP) and Tables, Figures and Listings (TFLs) to ensure appropriate data presentation for CSR purposes. Provide feedback on SAP and TFLs to project team as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Inform management of medical writing problems promptly and propose solutions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide advice on medical writing issues to project team members (internal and external) and help to resolve problems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent department in audits and interdepartmental working groups.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain in-depth scientific, medical, and technical knowledge relevant to Mirum’s clinical studies and pipeline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop strong relationships with external advisors.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;An advanced degree with minimum of 8-10 years of experience in medical writing in the pharmaceutical, biotech, medical communication agency industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent writing ability with strong editorial and formatting skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Fluency in written and spoken English.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An independently motivated working style with good problem-solving skills that allow analysis, synthesis, and compilation of data from a broad range of disciplines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing vendors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Rare disease or liver disease background highly desirable.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Have a demonstrated ability to produce clear, concise, and effective written and verbal communications describing scientific and clinical data in English.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An ability to work in a fast-paced, cohesive, collaborative team-oriented work environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-directed and solution oriented.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive knowledge of FDA and ICH regulations and guidelines, as well as familiarity of AMA Style Guide and Chicago Manual of Style.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong proficiency in Word, Excel, PowerPoint, and other applications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to demonstrate a familiarity with principles of clinical research and interpret and present clinical data and other complex information.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A demonstrated ability to prioritize tasks, work simultaneously on multiple projects, and complete high-quality documents according to timelines.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $230,000 to $245,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033161007,"name":"Regulatory Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5138064007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4632588007,"location":{"name":"Foster City"},"metadata":null,"id":5138064007,"updated_at":"2026-06-02T18:27:00-04:00","requisition_id":"2026-MAY-026","title":"Director, Publications","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-19T17:46:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director of Publications manages external publication vendors as well as edits medically relevant scientific presentations (i.e., clinical, scientific, and health economics, abstracts, posters, and oral presentations) to fulfill scientific and medical objectives, in accordance with authors’ direction and in adherence to Publication Policy Procedures and ICMJE and GPP3 guidelines. Assists with the creation of other scientific documents (e.g., medical science liaison [MSL] training slide decks, training tools, and FAQs). Communicates effectively with external authors and internal stakeholders and presents project updates to Sr. Director VLX GMAT Team, Executive Director, Publications, Executive Director, Medical Affairs, Senior Vice President of Medical Affairs, and Mirum Senior Leadership.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Key Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Understand scientific and medical content in given areas of the company.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and edit scientific content for oral and poster presentations at congresses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage publications vendor and work closely with key internal and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement the publication management system (Datavision).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Development of scientific training tactics (eg, internal training MSL decks, tools, FAQs).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engage internal and external subject matter experts, when appropriate, for participation in scientific communication tactics and content development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage and contribute to global publication and scientific communications plans for the company needs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Other Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Work effectively with our Medical Communications Agency on publication strategies and deliverables.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Learn and apply knowledge of therapeutic area data to scientific publishing projects focused on congress presentations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operationally execute all activities to agreed timelines related to the preparation of scientific medical publications (i.e., medical, scientific, and health economics abstracts, posters, and oral presentations).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with Medical Legal and Regulatory (MLR) Committee review and approvals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interface with external experts (e.g., physicians, other health care professionals) and effectively collaborate with Clinical Research and Development colleagues, along with other Mirum stakeholders including, but not limited to, Compliance, Safety, Biostatistics, Clinical Operations, and the Commercial group to ensure accurate and timely completion/delivery of information, including addressing conflicting demands, and review of scientific presentations and training programs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree with 5-7+ yrs. experience in scientific communication, training, and/or publications planning and development in an agency or pharmaceutical environment or applicable experience working in pharmaceutical environment with transferable skill set.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated strong project management skills and leadership poise a must to negotiate and facilitate alignment amongst internal and external stakeholders (KOLs, authors, cross functional teams).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with cross-functional stakeholders and/or agencies to develop abstracts, posters, and oral presentations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent and effective interpersonal and communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be well organized and able to multi-task in a fast-paced deadline driven environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience managing vendors and budgets.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;Knowledge, Skills and Abilities:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced computer and Internet skills, including knowledge of MS applications such as Word, PowerPoint, Excel, Veeva RIM, electronic publication management tools (e.g., PubStrat and Datavision), references databases (e.g., EndNote), PubMed, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel (US and International) approximately 30% of time.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $220,000 to $235,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033160007,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5058568007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4595608007,"location":{"name":"Foster City"},"metadata":null,"id":5058568007,"updated_at":"2026-06-02T19:26:00-04:00","requisition_id":"2026-INC-010","title":"Executive Director, Clinical Development","company_name":"Mirum Pharmaceuticals","first_published":"2026-02-20T18:08:57-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Executive Director, Clinical Development will join the Clinical Development group and will be responsible for all clinical trial related activities in all stages of clinical development in a cross-functional team of internal and external experts, investigators and government agencies. Activities include but are not limited to protocol development, support study startup, oversight of trial execution, recruitment, ongoing clinical development management and closeout as appropriate. Compliance with internal processes, GCP/ICH and regulatory requirements, study and data monitoring, data analysis, are required. Participation in health authority meetings and regulatory filing activities are also part of this role. The Director, Clinical Development, operates in collaboration with other functions including internal Safety and Clinical Operations teams.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Leadership and management of all aspects of complex, global development clinical study program(s), from phase 1 through registration globally.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Primary point of contact for medical inquiries from sites, CRO and site monitors; answer or triage questions as appropriate integration of clinical/regulatory strategy into global product development strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Primary liaison for internal Clinical Operations for site selection, site start-up activities, study management and closeout activities, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the creation of and/or review of clinical slides for internal and external meetings (i.e. Investigator Meetings, SIVs, Advisory Boards, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in authoring key clinical study documents, including Protocols, Clinical Study Reports, Investigator Brochures, Regulatory Authority briefing books, Development Safety Update Reports etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for medical monitoring of efficacy and safety clinical trial data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic input on the overall development plan, internal and external evaluation of new indications and studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversight of medical aspects of compliance of and inspection readiness in completed, ongoing and starting clinical trials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaboration in the analysis and writing of scientific publications/presentations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Works closely with other functions, in particular with Safety function and Clinical Operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Co-leads Study Management Team with Clinical Operations lead.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;MD, with a minimum of ≥5years.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in rare disease.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge and understanding of regulatory requirements for product approval and compliance in US and Europe.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;KNOWLEDGE, SKILLS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated accountability for delivery on complex development plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leadership in clinical development programs and multidisciplinary trial teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with basic statistical principles and techniques of data analysis, interpretation and clinical relevance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to understand and communicate risks, as well as develop and execute contingency plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience presenting data to regulatory agencies and advisory committees.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to think creatively and develop and execute in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail oriented with exceptional organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective communicator with strong verbal and written skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026amp;nbsp;Ability to identify issues, analyze situations and provide effective solutions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of the clinical development process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of applicable regulatory guidance.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Environment:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;This is a high growth, fast paced organization. The ability to be productive and successful in a work environment is critical.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness and ability to travel domestically and internationally is required, it is anticipated that this will be 30% of work time.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p class=\u0026quot;pf0\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;cf0\u0026quot;\u0026gt;The salary range for this position is $375,000 to $420,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;pf0\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;cf0\u0026quot;\u0026gt;#LI-HYBRID\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033162007,"name":"R\u0026D","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5155106007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4640913007,"location":{"name":"Foster City"},"metadata":null,"id":5155106007,"updated_at":"2026-06-04T16:47:43-04:00","requisition_id":"2026-MAY-012","title":"Patient Navigator","company_name":"Mirum Pharmaceuticals","first_published":"2026-06-04T16:45:00-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you someone who has the proven ability to thrive in a dynamic, evolving environment and contribute to building new capabilities in healthcare. We’re seeking an empathetic, detail-driven\u0026amp;nbsp;Patient Navigator to join our growing rare disease team. In this pivotal role, you’ll serve as the primary liaison for patients, caregivers, and healthcare providers, ensuring a seamless experience from prescription to ongoing therapy.\u0026amp;nbsp; You will provide inbound and outbound phone support and serve as the primary contact for patients, caregivers, and providers. You will facilitate a collaborative process that gauges, coordinates, and monitors patient need and appropriately facilitates a patient’s journey utilizing services offered through the Patient Support Program on behalf of Mirum and coordination with our specialty pharmacy partner. You’ll work closely with the specialty pharmacy, reimbursement specialists, and internal partners to make sure patients receive their medications on time, every time.\u0026amp;nbsp;The outcome of your efforts will be providing unparalleled customer service to patients, caregivers and,\u0026amp;nbsp; providers.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you have a nursing or case management background, can thrive in a fast-paced biotech environment, and are passionate about helping patients with rare diseases navigate complex access barriers—this is the opportunity for you.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;main point of contact for patients and caregivers, providing non-clinical guidance and emotional support throughout their treatment journey demonstrating a thorough understanding of the disease state and Mirum product profiles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide patients and HCPs a clear understanding of eligibility requirements, program enrollment, reimbursement process, affordability support, and general access for Mirum prescribed therapies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deliver unparalleled customer service while serving as a brand advocate and program representative; understands the importance of achieving quality outcomes and commit to the appropriate use of resources\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate care between prescribers, specialty pharmacies, and insurance providers to ensure timely drug access and refills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor patient cases to identify potential delays or issues (e.g., prior authorizations, benefit revalidations, prescription renewals) and proactively resolve them.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Educate patients and families about program resources, refill schedules, and financial assistance options.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Elevate the patient experience by partnering with Mirum’s market access, reimbursement, and specialty pharmacy teams to resolve coverage and dispensing challenges.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support patient onboarding, therapy continuation, and adherence initiatives in alignment with program KPIs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a resource for patients and healthcare professionals to verify insurance coverage, reimbursement process, and general access for complex pharmaceuticals and ability to understand and explain benefits offered by all payer types including private/commercial and government (i.e., Medicare, Medicaid, VA and DOD)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Patient Navigators will be regionally aligned and will serve as an expert on reimbursement, co-pay, foundation assistance, patient assistance program (PAP) issues, and other forms of available support and will be responsible for handling patient and healthcare provider interactions related to these topics in collaboration with the Regional Access Leads and Regional Account Managers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for communicating insurance benefit investigations, prior authorization and appeal requirements, and triage cases according to program standard operating procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as direct point of contact to health care providers for ongoing support and relationship development by acquiring and delivering detailed information regarding a program and/or a patient\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate program enrollment forms for data integrity and missing information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Follow program guidelines and escalate complex cases according to program policy, SOPs, Call Guides, and other program materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working in a case management system, documenting status/background in case notes, communicating patient benefits, assisting in the PA/Appeals process and like responsibilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as an assigned liaison to customer contacts (e.g., regional contact for sales representatives), Market Access colleagues, other internal stakeholders and healthcare providers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Works with the Program Supervisor, on a day-to-day basis to maintain open lines of communication and share awareness regarding patient status, prescriber feedback/satisfaction and program effectiveness\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains a high level of ethical conduct regarding confidentiality and privacy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help maintain team morale by consistently demonstrating positive attitude.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate, compliant documentation within CRM and case management systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conducts miscellaneous tasks or projects as assigned identify and report pharmacovigilance information as required, i.e., Adverse Events, and Product Quality Complaints\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BA/BS Highly Desired.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Registered Nurse (RN), Licensed Practical Nurse (LPN/LVN) Social Worker (BSW), PharmD, RPh, or equivalent pharmacist credential, Pharmacy Technician certification (CPhT) or Case Manager (CCM) preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 5+ years of experience in patient navigation, specialty pharmacy, case management, or patient access (biotech or rare disease experience highly preferred) preferably in rare disease, oncology or cell/gene therapy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding and experience in working through benefits verification, prior authorization, and reimbursement processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional communication, organization, and problem-solving skills that have been demonstrating in producing improved patient experiences and outcomes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to work independently in a high-volume, fast paced and patient-focused environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Empathetic and patient-centered mindset with a commitment to improving rare disease care.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to multitask and balance multiple priorities at once.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to deliver meaningful \u0026amp;amp; concise conversations with integrity and empathy directly to patients and health care providers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using CRM or case tracking systems (Salesforce Health Cloud preferred)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth understanding of health insurance benefits, relevant state and federal laws and insurance regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and oral communication, and problem-solving skills, including the ability to connect with patients, caregivers, and providers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience and demonstrated success working in a complex matrix to accomplish goals with a patient centric approach.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong people skills that demonstrate flexibility, persistence, creativity, empathy, and trust.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Robust computer literacy skills including data entry and MS Office-based software programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possesses strong business acumen and strategic thinking skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to identify and handle sensitive issues, working independently and collaboratively within teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel required, ~10%, possibly weekends.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This position is based in Foster City, CA. Applicants must reside in a location which would allow them to comply with Mirum’s hybrid work policy.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $125,000 to $140,000USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5155100007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4640911007,"location":{"name":"Charlotte, NC"},"metadata":null,"id":5155100007,"updated_at":"2026-06-04T18:55:04-04:00","requisition_id":"2026-MAY-013","title":"Patient Navigator","company_name":"Mirum Pharmaceuticals","first_published":"2026-06-04T16:46:27-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you someone who has the proven ability to thrive in a dynamic, evolving environment and contribute to building new capabilities in healthcare. We’re seeking an empathetic, detail-driven\u0026amp;nbsp;Patient Navigator to join our growing rare disease team. In this pivotal role, you’ll serve as the primary liaison for patients, caregivers, and healthcare providers, ensuring a seamless experience from prescription to ongoing therapy.\u0026amp;nbsp; You will provide inbound and outbound phone support and serve as the primary contact for patients, caregivers, and providers. You will facilitate a collaborative process that gauges, coordinates, and monitors patient need and appropriately facilitates a patient’s journey utilizing services offered through the Patient Support Program on behalf of Mirum and coordination with our specialty pharmacy partner. You’ll work closely with the specialty pharmacy, reimbursement specialists, and internal partners to make sure patients receive their medications on time, every time.\u0026amp;nbsp;The outcome of your efforts will be providing unparalleled customer service to patients, caregivers and,\u0026amp;nbsp; providers.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you have a nursing or case management background, can thrive in a fast-paced biotech environment, and are passionate about helping patients with rare diseases navigate complex access barriers—this is the opportunity for you.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;main point of contact for patients and caregivers, providing non-clinical guidance and emotional support throughout their treatment journey demonstrating a thorough understanding of the disease state and Mirum product profiles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide patients and HCPs a clear understanding of eligibility requirements, program enrollment, reimbursement process, affordability support, and general access for Mirum prescribed therapies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deliver unparalleled customer service while serving as a brand advocate and program representative; understands the importance of achieving quality outcomes and commit to the appropriate use of resources\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate care between prescribers, specialty pharmacies, and insurance providers to ensure timely drug access and refills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor patient cases to identify potential delays or issues (e.g., prior authorizations, benefit revalidations, prescription renewals) and proactively resolve them.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Educate patients and families about program resources, refill schedules, and financial assistance options.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Elevate the patient experience by partnering with Mirum’s market access, reimbursement, and specialty pharmacy teams to resolve coverage and dispensing challenges.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support patient onboarding, therapy continuation, and adherence initiatives in alignment with program KPIs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a resource for patients and healthcare professionals to verify insurance coverage, reimbursement process, and general access for complex pharmaceuticals and ability to understand and explain benefits offered by all payer types including private/commercial and government (i.e., Medicare, Medicaid, VA and DOD)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Patient Navigators will be regionally aligned and will serve as an expert on reimbursement, co-pay, foundation assistance, patient assistance program (PAP) issues, and other forms of available support and will be responsible for handling patient and healthcare provider interactions related to these topics in collaboration with the Regional Access Leads and Regional Account Managers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for communicating insurance benefit investigations, prior authorization and appeal requirements, and triage cases according to program standard operating procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as direct point of contact to health care providers for ongoing support and relationship development by acquiring and delivering detailed information regarding a program and/or a patient\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate program enrollment forms for data integrity and missing information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Follow program guidelines and escalate complex cases according to program policy, SOPs, Call Guides, and other program materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working in a case management system, documenting status/background in case notes, communicating patient benefits, assisting in the PA/Appeals process and like responsibilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as an assigned liaison to customer contacts (e.g., regional contact for sales representatives), Market Access colleagues, other internal stakeholders and healthcare providers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Works with the Program Supervisor, on a day-to-day basis to maintain open lines of communication and share awareness regarding patient status, prescriber feedback/satisfaction and program effectiveness\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains a high level of ethical conduct regarding confidentiality and privacy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help maintain team morale by consistently demonstrating positive attitude.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate, compliant documentation within CRM and case management systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conducts miscellaneous tasks or projects as assigned identify and report pharmacovigilance information as required, i.e., Adverse Events, and Product Quality Complaints\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BA/BS Highly Desired.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Registered Nurse (RN), Licensed Practical Nurse (LPN/LVN) Social Worker (BSW), PharmD, RPh, or equivalent pharmacist credential, Pharmacy Technician certification (CPhT) or Case Manager (CCM) preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 5+ years of experience in patient navigation, specialty pharmacy, case management, or patient access (biotech or rare disease experience highly preferred) preferably in rare disease, oncology or cell/gene therapy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding and experience in working through benefits verification, prior authorization, and reimbursement processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional communication, organization, and problem-solving skills that have been demonstrating in producing improved patient experiences and outcomes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to work independently in a high-volume, fast paced and patient-focused environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Empathetic and patient-centered mindset with a commitment to improving rare disease care.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to multitask and balance multiple priorities at once.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to deliver meaningful \u0026amp;amp; concise conversations with integrity and empathy directly to patients and health care providers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using CRM or case tracking systems (Salesforce Health Cloud preferred)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth understanding of health insurance benefits, relevant state and federal laws and insurance regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and oral communication, and problem-solving skills, including the ability to connect with patients, caregivers, and providers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience and demonstrated success working in a complex matrix to accomplish goals with a patient centric approach.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong people skills that demonstrate flexibility, persistence, creativity, empathy, and trust.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Robust computer literacy skills including data entry and MS Office-based software programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possesses strong business acumen and strategic thinking skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to identify and handle sensitive issues, working independently and collaboratively within teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel required, ~10%, possibly weekends.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This position is based in Charlotte, NC. Applicants must reside in a location which would allow them to comply with Mirum’s hybrid work policy.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4054753007,"name":"Charlotte","location":"North Carolina, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5130697007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4628858007,"location":{"name":"US Remote"},"metadata":null,"id":5130697007,"updated_at":"2026-06-02T19:27:12-04:00","requisition_id":"2026-MAY-007","title":"Regional Account Manager, Carolinas","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-06T17:05:10-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The \u0026lt;strong\u0026gt;Regional Account Manager, Carolinas (RAM)\u0026lt;/strong\u0026gt; is a key field position and will have the opportunity to run their own business within their assigned region. Reporting to the Area Business Director, East, this individual will possess experience in business ownership, leadership, analytics, and the implementation of innovative solutions. The RAM will formulate an effective regional strategy focusing on Geneticist, Endocrinology, and Metabolic Specialist as their core customers.\u0026amp;nbsp; They will be tasked with establishing short- and long-term business tactics. It will be the responsibility of the RAM to identify key priorities within territories and create and implement business plan that is organizationally approved and fully compliant with all laws. The RAM will be accountable for improving diagnosis rates of all on label indications within their region, growing sales, and effectively partnering across the organization to ensure all goals are met.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The successful RAM will have courage, talent and dedication to seek solutions that can make a meaningful impact within territory or broader team. The ideal candidates are detail orientated, self-structured in their approach to their work, with the ability to manage relationships at all levels. The RAM will have proven presentation and partner management skills and thrive in a rapid paced and dynamic environment within a culture that relies on a patient centric and teamwork orientated approach.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You must reside in one of the following states:\u0026amp;nbsp;South NC, SC, GA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Understands and effectively communicates complex scientific information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develops and implements strategic region-level business plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborates cross-functionally with internal stakeholders (e.g., Marketing, Market Access, Medical, Operations, Compliance)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drives innovative, accountable, and entrepreneurial approaches to business challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates strong organizational and time management skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exhibits a strong commitment to customer experience and standards of excellence\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Applies strong business acumen to inform decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates high integrity and adherence to compliance standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates adaptability and effectiveness in fast-paced, dynamic, and collaborative environments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; MBA or advanced degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5+ years of experience in the pharmaceutical/biotech industry, including 3 years of field-based experience in account management, sales, and/or field reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in specialty, genetics, or rare disease markets strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success in product launches, ideally with first-in-class therapies and in competitive markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience navigating complex rare disease patient journeys, including diagnosis, referral pathways, and access challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in ambiguous environments requiring cross-specialty coordination for patient identification\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing a large multi-state geography preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel frequently (up to 70% overnight) and maintain a valid driver’s license\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-REMOTE\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4032948007,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5148074007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4637478007,"location":{"name":"US Remote"},"metadata":null,"id":5148074007,"updated_at":"2026-06-02T19:28:03-04:00","requisition_id":"2026-REP-022","title":"Regional Account Manager, Keystone ","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-28T17:50:39-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The \u0026lt;strong\u0026gt;Regional Account Manager, Keystone (RAM)\u0026lt;/strong\u0026gt; is a key field position and will have the opportunity to run their own business within their assigned region. Reporting to the Area Business Director, East, this individual will possess experience in business ownership, leadership, analytics, and the implementation of innovative solutions. The RAM will formulate an effective regional strategy focusing on Geneticist, Endocrinology, and Metabolic Specialist as their core customers.\u0026amp;nbsp; They will be tasked with establishing short- and long-term business tactics. It will be the responsibility of the RAM to identify key priorities within territories and create and implement business plan that is organizationally approved and fully compliant with all laws. The RAM will be accountable for improving diagnosis rates of all on label indications within their region, growing sales, and effectively partnering across the organization to ensure all goals are met.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The successful RAM will have courage, talent and dedication to seek solutions that can make a meaningful impact within territory or broader team. The ideal candidates are detail orientated, self-structured in their approach to their work, with the ability to manage relationships at all levels. The RAM will have proven presentation and partner management skills and thrive in a rapid paced and dynamic environment within a culture that relies on a patient centric and teamwork orientated approach.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You must reside in one of the following states: PA, NJ, DE\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Understands and effectively communicates complex scientific information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develops and implements strategic region-level business plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborates cross-functionally with internal stakeholders (e.g., Marketing, Market Access, Medical, Operations, Compliance)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drives innovative, accountable, and entrepreneurial approaches to business challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates strong organizational and time management skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exhibits a strong commitment to customer experience and standards of excellence\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Applies strong business acumen to inform decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates high integrity and adherence to compliance standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates adaptability and effectiveness in fast-paced, dynamic, and collaborative environments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; MBA or advanced degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5+ years of experience in the pharmaceutical/biotech industry, including 3 years of field-based experience in account management, sales, and/or field reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in specialty, genetics, or rare disease markets strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success in product launches, ideally with first-in-class therapies and in competitive markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience navigating complex rare disease patient journeys, including diagnosis, referral pathways, and access challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in ambiguous environments requiring cross-specialty coordination for patient identification\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing a large multi-state geography preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel frequently (up to 70% overnight) and maintain a valid driver’s license\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-REMOTE\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4032948007,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5130683007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4628851007,"location":{"name":"US Remote"},"metadata":null,"id":5130683007,"updated_at":"2026-06-02T19:29:00-04:00","requisition_id":"2026-MAY-008","title":"Regional Account Manager, Ohio Valley","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-06T17:05:31-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The \u0026lt;strong\u0026gt;Regional Account Manager, Ohio Valley (RAM)\u0026lt;/strong\u0026gt; is a key field position and will have the opportunity to run their own business within their assigned region. Reporting to the Area Business Director, East, this individual will possess experience in business ownership, leadership, analytics, and the implementation of innovative solutions. The RAM will formulate an effective regional strategy focusing on Geneticist, Endocrinology, and Metabolic Specialist as their core customers.\u0026amp;nbsp; They will be tasked with establishing short- and long-term business tactics. It will be the responsibility of the RAM to identify key priorities within territories and create and implement business plan that is organizationally approved and fully compliant with all laws. The RAM will be accountable for improving diagnosis rates of all on label indications within their region, growing sales, and effectively partnering across the organization to ensure all goals are met.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The successful RAM will have courage, talent and dedication to seek solutions that can make a meaningful impact within territory or broader team. The ideal candidates are detail orientated, self-structured in their approach to their work, with the ability to manage relationships at all levels. The RAM will have proven presentation and partner management skills and thrive in a rapid paced and dynamic environment within a culture that relies on a patient centric and teamwork orientated approach.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You must reside in one of the following states:\u0026amp;nbsp;MI, OH, North IN, WV\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Understands and effectively communicates complex scientific information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develops and implements strategic region-level business plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborates cross-functionally with internal stakeholders (e.g., Marketing, Market Access, Medical, Operations, Compliance)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drives innovative, accountable, and entrepreneurial approaches to business challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates strong organizational and time management skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exhibits a strong commitment to customer experience and standards of excellence\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Applies strong business acumen to inform decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates high integrity and adherence to compliance standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates adaptability and effectiveness in fast-paced, dynamic, and collaborative environments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; MBA or advanced degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5+ years of experience in the pharmaceutical/biotech industry, including 3 years of field-based experience in account management, sales, and/or field reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in specialty, genetics, or rare disease markets strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success in product launches, ideally with first-in-class therapies and in competitive markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience navigating complex rare disease patient journeys, including diagnosis, referral pathways, and access challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in ambiguous environments requiring cross-specialty coordination for patient identification\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing a large multi-state geography preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel frequently (up to 70% overnight) and maintain a valid driver’s license\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-REMOTE\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4032948007,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5130576007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4628805007,"location":{"name":"US Remote"},"metadata":null,"id":5130576007,"updated_at":"2026-06-02T19:29:54-04:00","requisition_id":"2026-MAY-009","title":"Regional Account Manager, South Central","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-06T17:05:41-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The \u0026lt;strong\u0026gt;Regional Account Manager, South Central (RAM)\u0026lt;/strong\u0026gt; is a key field position and will have the opportunity to run their own business within their assigned region. Reporting to the Area Business Director, West, this individual will possess experience in business ownership, leadership, analytics, and the implementation of innovative solutions. The RAM will formulate an effective regional strategy focusing on Geneticist, Endocrinology, and Metabolic Specialist as their core customers.\u0026amp;nbsp; They will be tasked with establishing short- and long-term business tactics. It will be the responsibility of the RAM to identify key priorities within territories and create and implement business plan that is organizationally approved and fully compliant with all laws. The RAM will be accountable for improving diagnosis rates of all on label indications within their region, growing sales, and effectively partnering across the organization to ensure all goals are met.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The successful RAM will have courage, talent and dedication to seek solutions that can make a meaningful impact within territory or broader team. The ideal candidates are detail orientated, self-structured in their approach to their work, with the ability to manage relationships at all levels. The RAM will have proven presentation and partner management skills and thrive in a rapid paced and dynamic environment within a culture that relies on a patient centric and teamwork orientated approach.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You must reside in one of the following states:\u0026amp;nbsp;OK, West MO, AR, LA, EastTX\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Understands and effectively communicates complex scientific information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develops and implements strategic region-level business plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborates cross-functionally with internal stakeholders (e.g., Marketing, Market Access, Medical, Operations, Compliance)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drives innovative, accountable, and entrepreneurial approaches to business challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates strong organizational and time management skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exhibits a strong commitment to customer experience and standards of excellence\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Applies strong business acumen to inform decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates high integrity and adherence to compliance standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates adaptability and effectiveness in fast-paced, dynamic, and collaborative environments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; MBA or advanced degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5+ years of experience in the pharmaceutical/biotech industry, including 3 years of field-based experience in account management, sales, and/or field reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in specialty, genetics, or rare disease markets strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success in product launches, ideally with first-in-class therapies and in competitive markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience navigating complex rare disease patient journeys, including diagnosis, referral pathways, and access challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in ambiguous environments requiring cross-specialty coordination for patient identification\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing a large multi-state geography preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel frequently (up to 70% overnight) and maintain a valid driver’s license\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-REMOTE\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4032948007,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5149458007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4638153007,"location":{"name":"US Remote"},"metadata":null,"id":5149458007,"updated_at":"2026-06-02T19:31:03-04:00","requisition_id":"2026-REP-024","title":"Regional Account Manager, Southern California","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-29T09:55:56-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The \u0026lt;strong\u0026gt;Regional Account Manager, Southern California (RAM)\u0026lt;/strong\u0026gt; is a key field position and will have the opportunity to run their own business within their assigned region. Reporting to the Area Business Director, West, this individual will possess experience in business ownership, leadership, analytics, and the implementation of innovative solutions. The RAM will formulate an effective regional strategy focusing on Geneticist, Endocrinology, and Metabolic Specialist as their core customers.\u0026amp;nbsp; They will be tasked with establishing short- and long-term business tactics. It will be the responsibility of the RAM to identify key priorities within territories and create and implement business plan that is organizationally approved and fully compliant with all laws. The RAM will be accountable for improving diagnosis rates of all on label indications within their region, growing sales, and effectively partnering across the organization to ensure all goals are met.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The successful RAM will have courage, talent and dedication to seek solutions that can make a meaningful impact within territory or broader team. The ideal candidates are detail orientated, self-structured in their approach to their work, with the ability to manage relationships at all levels. The RAM will have proven presentation and partner management skills and thrive in a rapid paced and dynamic environment within a culture that relies on a patient centric and teamwork orientated approach.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You must reside in one of the following states: SoCal, HI, NV\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Understands and effectively communicates complex scientific information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develops and implements strategic region-level business plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborates cross-functionally with internal stakeholders (e.g., Marketing, Market Access, Medical, Operations, Compliance)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drives innovative, accountable, and entrepreneurial approaches to business challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates strong organizational and time management skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exhibits a strong commitment to customer experience and standards of excellence\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Applies strong business acumen to inform decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates high integrity and adherence to compliance standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates adaptability and effectiveness in fast-paced, dynamic, and collaborative environments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; MBA or advanced degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5+ years of experience in the pharmaceutical/biotech industry, including 3 years of field-based experience in account management, sales, and/or field reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in specialty, genetics, or rare disease markets strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success in product launches, ideally with first-in-class therapies and in competitive markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience navigating complex rare disease patient journeys, including diagnosis, referral pathways, and access challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in ambiguous environments requiring cross-specialty coordination for patient identification\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing a large multi-state geography preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel frequently (up to 70% overnight) and maintain a valid driver’s license\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-REMOTE\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4032948007,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5135445007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4631297007,"location":{"name":"US Remote"},"metadata":null,"id":5135445007,"updated_at":"2026-06-02T19:13:54-04:00","requisition_id":"2026-MAY-041","title":"Sales Director, HDV Business Unit","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-12T12:35:52-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Sales Director, HDV Business Unit will lead a highly specialized field team of Regional Account Managers (RAMs) tasked with preparing the U.S. market for the anticipated launch of\u0026amp;nbsp;\u0026lt;strong\u0026gt;Brelovitug\u0026lt;/strong\u0026gt; for Hepatitis Delta Virus (HDV), pending regulatory approval. This role is responsible for advancing disease awareness, supporting account readiness, and helping to establish the foundation for appropriate patient identification and management in a market with profound unmet need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;HDV represents the most severe form of viral hepatitis, requiring Hepatitis B co-infection for replication and spread. Despite an estimated U.S. prevalence of ~40,000 patients and ~15,000 who are diagnosed, insured, and under care, there are currently no approved therapies in the U.S., underscoring the urgency and importance of this role.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This leader must excel at operating in ambiguity—defining strategy, building structure, and driving execution in a market that is still being shaped in real time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Strategic Leadership\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Build and lead the HDV team of 6 Regional Account Managers across key U.S. geographies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute a pre-launch market development strategy focused on HDV disease awareness and diagnosis expansion\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and prioritize high-value accounts within key HDV geographies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translate evolving epidemiology, market insights, and competitive dynamics into actionable, compliant field strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create clarity from ambiguity by setting direction, establishing priorities, and adapting strategy as new information emerges\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Market Development \u0026amp;amp; Disease Education\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Drive awareness of HDV as a severe, underdiagnosed condition requiring urgent intervention\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expand understanding of the relationship between HDV and Hepatitis B (HBsAg dependency)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with KOLs and key institutions to support HDV screening, diagnosis, and referral pathways\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support initiatives to improve patient identification within the estimated ~40,000 patients under care\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Account Engagement \u0026amp;amp; Activation\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure strategic engagement across key stakeholders and health systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish account plans focused on screening protocols, care pathways, and disease management readiness\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate cross-functionally with Medical Affairs, Market Access, and Marketing to ensure aligned execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support accounts in enhancing (or operationalizing) HDV identification and management in the absence of established standards\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Team Leadership \u0026amp;amp; Development\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Recruit, develop, and coach a high-impact team of RAMs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Set clear expectations aligned with pre-launch, non-promotional objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster a culture of accountability, agility, and mission-driven execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coach the team to operate effectively without fixed playbooks—encouraging problem-solving, adaptability, and proactive compliant decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead through influence in a complex, cross-functional environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Cross-Functional Collaboration\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the field leadership voice in launch planning\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical Affairs on scientific exchange and KOL engagement (as appropriate and compliant)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Market Access on payer readiness and coverage considerations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commercial leadership on launch readiness and execution\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Align stakeholders around evolving strategies, even when data, timelines, or market conditions are still emerging\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; MBA or advanced degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;7+ years of pharmaceutical/biotech experience, including field leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success leading account-based or specialty field teams through ambiguity\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in rare disease, hepatology, infectious disease, or specialty launches\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to build strategy in pre-launch environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of U.S. healthcare systems, IDNs, and academic centers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Hepatitis B, liver disease, or transplant networks preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Launch experience in a market with low awareness/high unmet need\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong KOL engagement and scientific fluence\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thrives in a fast-paced, dynamic, and collaborative environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to travel frequently, up to 70% overnight travel and has a valid drivers’ license\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;KEY COMPETENCIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strategic thinker with strong execution discipline\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfort leading through ambiguity—able to make decisions with incomplete information and adjust rapidly\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to build structure and momentum from the ground up\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional leadership and team development skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High emotional intelligence and stakeholder influence\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mission-driven mindset aligned to addressing critical unmet need\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to understand and effectively communicate scientific information within role and scope\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster a culture of innovation, accountability, and entrepreneurial thinking\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-REMOTE\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4032948007,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5124380007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4625941007,"location":{"name":"Foster City"},"metadata":null,"id":5124380007,"updated_at":"2026-06-02T19:32:19-04:00","requisition_id":"2026-REP-016","title":"Senior Director, CMC Project Management","company_name":"Mirum Pharmaceuticals","first_published":"2026-04-30T13:30:56-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are looking for a Senior Director of CMC Project Management who is upbeat, organized, self-motivated, collaborative, detail-oriented, and has a strong technical background and knowledge base. \u0026amp;nbsp;The person filling this player/coach role will\u0026amp;nbsp;partner with the Head of Tech Ops, Biologics to provide strategic and operational leadership\u0026amp;nbsp;to the brelovitug CMC program, overseeing the development and implementation of integrated CMC plans from PPQ campaigns through global regulatory submission, approval, commercial launch, and lifecycle management activities. This role requires being able to prioritize to meet both short-term and long-term goals. This is a fantastic opportunity to make an impact, wear many hats, and be a part of an exciting growing biotech company.\u0026amp;nbsp; This position is located in Foster City.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage program CMC budgets and related contracts, partnering with internal Finance and Contract functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary business lead for external partners, ensuring technical transfers, \u0026amp;nbsp;manufacturing campaigns, testing, and other externally sourced activities stay on schedule and within budget.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain dashboards and reporting mechanisms for program status, risks, decisions, and critical path updates for team and senior/executive leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate cross-functional communications to gather inputs, align priorities, resolve conflicts, and share project updates; ensure clarity of owners, deliverables, and deadlines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain an integrated program timeline identifying critical decision points, governance reviews, team events, and key milestones.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Program Project Management to ensure appropriate integration with overall product strategy, timelines, and reporting, including alignment between development activities and portfolio-level planning as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support preparation for governance reviews and executive program presentations, ensuring materials are accurate, aligned, decision-oriented, and delivered on schedule.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive disciplined change control and documentation of scope/timeline changes, ensuring impacts are understood and communicated to stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree; advanced degree (M.S., Ph.D, or MBA) preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;At least 15+ years of work experience in the pharmaceutical/biotech industry with a significant focus on CMC project management for biologics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing relationships with biologics CDMOs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to effectively communicate updates, issues, and strategic solutions to problems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;PMP (Project Management Professional) or equivalent accreditation is desired.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;KNOWLEDGE, SKILLS, AND ABILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills and ability to collaborate across functions; proven ability to influence without authority.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong PM fundamentals (meeting management, timeline/critical path management, risk and issue management, decision tracking, action management, governance preparation).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive, forward-thinking, and able to anticipate needs in dynamic environments with competing priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional facilitation and communication skills (including executive-ready written and presentation skills) with success influencing at all levels cross-functionally.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic, able to identify long term needs and risks and to incorporate these into a long-term plan. Proven ability to make smart business decisions while balancing scientific, technical, and risk-based factors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly collaborative with outstanding relationship-building skills; ability to lead teams, navigate ambiguity, and resolve conflict effectively.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with project/portfolio management tools and systems and strong working knowledge of common collaboration tools (e.g., MS Office, Smartsheet, SharePoint).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willing to travel and to participate in teleconferences during non-business hours.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $270,000 to $300,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033162007,"name":"R\u0026D","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5108395007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4618352007,"location":{"name":"Foster City"},"metadata":null,"id":5108395007,"updated_at":"2026-06-02T19:33:47-04:00","requisition_id":"2026-MAY-003","title":"Senior Director, Development Quality (GMP)","company_name":"Mirum Pharmaceuticals","first_published":"2026-04-14T18:30:50-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking an experienced\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;Senior Director, Development Quality (GMP) who will be responsible for providing strategic and operational quality oversight for product development activities from early development through commercialization. This role ensures compliance with global GMP regulations and supports development, scale-up, and technology transfer of drug substance, drug product, and finished product.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position requires extensive experience in GMP Quality Assurance, including oversight of CMC development, clinical manufacturing, and global supply, along with strong knowledge of regulatory expectations across all phases of development..\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as a strategic Quality leader to support development and advancement of a compliant, phase-appropriate, and collaborative GMP quality culture across development and technical operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide QA oversight of product development lifecycle activities, including drug substance (DS), drug product (DP), and finished product (FP) from early development through commercialization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee and support GMP quality systems applicable to development, including deviations, CAPAs, change control, investigations, and product complaints.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide QA support for clinical manufacturing, including batch record review/disposition and release of DS, DP, and FP for clinical use.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure quality oversight of process development, technology transfer, scale-up, and validation activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support preparation, review, and approval of CMC sections for regulatory submissions (e.g., IND, NDA, MAA) and responses to regulatory authority questions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interface with regulatory agencies and support GMP inspections, including pre-approval inspections (PAIs) and general GMP inspections.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify compliance risks within development and manufacturing activities and escalate issues to appropriate levels of management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee and support GMP vendor management, including qualification, auditing, and ongoing oversight of CMOs, laboratories, and suppliers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and maintain Quality/Technical Agreements with CMOs and development partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support new product introduction, acquisition, and integration activities from a GMP quality perspective.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support development and oversight of stability programs for investigational and commercial products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, track, and trend quality metrics for reporting to Quality Management Review (QMR) and Annual Product Reviews (APR/APQR).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure inspection readiness across development and clinical manufacturing operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate cross-functionally with Technical Operations, CMC, Regulatory Affairs, Supply Chain, and Manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build, mentor, and lead a high-performing Development Quality team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Champion a culture of quality and inspection readiness across internal and external operations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in a scientific discipline; advanced degree (MS, PhD) preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;15+ years of experience in the pharmaceutical/biotech industry, including 12+ years in GMP Quality Assurance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong expertise in global GMP regulations, including FDA, EMA (EudraLex), ICH guidelines, and Good Manufacturing Practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience supporting product development from early stage through commercialization, including clinical manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of CMC development, process validation, technology transfer, and manufacturing operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting regulatory submissions (IND, NDA, MAA) and health authority inspections, including PAIs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with GMP vendor oversight, including CMOs and contract laboratories.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven leadership experience with the ability to build and develop high-performing teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of pharmaceutical supply chain and lifecycle management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with inspection readiness and continuous improvement of quality systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, collaboration, and risk management skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of FDA, EMA, ROW CGMP regulations, and ICH guidance\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $275,657 to $310,847 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033155007,"name":"Quality Assurance","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/4941307007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4534373007,"location":{"name":"Foster City"},"metadata":null,"id":4941307007,"updated_at":"2026-06-02T19:34:48-04:00","requisition_id":"2025-SEP-001","title":"Senior Director, Intellectual Property Attorney","company_name":"Mirum Pharmaceuticals","first_published":"2025-10-10T16:16:31-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking an experienced \u0026lt;strong\u0026gt;Senior Director, Intellectual Property\u0026lt;/strong\u0026gt; to lead our intellectual property (IP) strategy in support of our mission to develop and commercialize transformative therapies for patients with rare diseases. This role reports to the Chief Legal Officer, requires a balance of strategic acumen and hands-on execution and will be responsible for shaping and executing a comprehensive global IP program across our clinical and commercial programs. As a senior legal leader in a dynamic, high-growth biopharmaceutical organization (~350 employees worldwide), you will partner closely with internal teams and outside counsel to maximize the value of our programs while mitigating risk.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;PRIMARY RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;IP Strategy \u0026amp;amp; Portfolio Management\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;In partnership with the Chief Legal Officer and outside intellectual property counsel, develop and oversee a global IP strategy for the company’s patents, trademarks and trade secrets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee the drafting, filing, prosecution, and maintenance of a worldwide patent portfolio.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide guidance on patent term extensions and regulatory exclusivities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deliver freedom-to-operate (FTO), patent validity, and infringement analyses to inform decision-making across development and commercial programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the company’s global trademark portfolio.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Transactional Support\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide IP guidance in business development, licensing, collaboration, and M\u0026amp;amp;A transactions; lead or support IP due diligence efforts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In collaboration with other Legal team members, draft and negotiate IP provisions in material agreements (e.g., research collaboration, license, clinical, supply, manufacturing and distribution agreements).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Litigation \u0026amp;amp; Disputes\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;With the Chief Legal Officer and outside counsel, manage potential Hatch-Waxman patent litigation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct and manage patent dispute processes such as U.S. inter partes review (IPR), post-grant proceedings, European oppositions, and other adversarial actions in key jurisdictions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support pre-litigation risk assessments.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Legal \u0026amp;amp; Business Support\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with program teams and internal functions to identify and capture inventions at an early stage.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate inventions and determine whether patent or trade secret protection would be appropriate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support product launches with lifecycle management strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;With the Chief Legal Officer, manage outside counsel relationships with a focus on cost-effectiveness and quality.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deliver timely, practical, and business-focused legal advice across jurisdictions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;J.D. and licensed to practice law in at least one U.S. jurisdiction (active and in good standing).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;USPTO registration and eligibility to practice patent law.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;12+ years of intellectual property law experience, with significant in-house and/or law firm experience in the biopharmaceutical sector.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced scientific degree (M.S. or Ph.D.) in chemistry, biochemistry or related discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong global perspective, with experience managing patent portfolios across the U.S., EU, UK and Japan.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record advising executives and program teams, balancing legal risk with business goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and oral communication skills — able to translate complex IP concepts for diverse stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with rare disease regulatory frameworks, including orphan drug exclusivity in the U.S. and EU.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success in managing patent litigation, disputes, oppositions, or post-grant proceedings.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;KNOWLEDGE, SKILLS, AND ABILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Mission-driven, passionate about bringing therapies to patients with serious, underserved rare diseases.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic thinker with hands-on execution ability in a small organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative, approachable and comfortable working cross-functionally in a fast-paced, global culture.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Entrepreneurial and creative mindset with flexibility to pivot quickly as business needs evolve.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong leadership presence, credibility, and collaborative mindset.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $315,000 to $335,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033156007,"name":"Corporate Functions","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5140730007","data_compliance":[{"type":"gdpr","requires_consent":true,"requires_processing_consent":true,"requires_retention_consent":true,"retention_period":365,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4633867007,"location":{"name":"Zug"},"metadata":null,"id":5140730007,"updated_at":"2026-06-01T18:46:25-04:00","requisition_id":"2026-REP-021","title":"Senior Director, International FP\u0026A","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-18T17:03:35-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Reporting to the Executive Director of FP\u0026amp;amp;A (based in US), the Senior Director, FP\u0026amp;amp;A – International will lead and own the financial planning and analysis function for Mirum’s International Commercial Operations. Based in Zug, this role serves as the primary finance partner to International leadership, with full accountability for financial performance, planning, and strategic decision support across Europe and expanding global markets.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This individual will play a critical role in building and scaling the international finance capability to support the commercialization of LIVMARLI and future pipeline assets. As a core member of the International leadership team, the role will drive financial visibility, inform strategic decisions, and ensure alignment between regional execution and global corporate objectives.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position combines strategic leadership with hands-on execution in a dynamic, growth-stage biotech environment and requires close collaboration with Commercial, Market Access, Supply Chain, R\u0026amp;amp;D, Legal, Compliance, HR, and global Finance teams.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;International Commercial Finance Leadership\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own and lead FP\u0026amp;amp;A for International Commercial Operations, with full accountability for regional P\u0026amp;amp;L performance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary finance partner to International leadership, influencing strategy, investment decisions, and operational execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a bridge between International markets and US headquarters, ensuring alignment with global financial goals and expectations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and evolve the international FP\u0026amp;amp;A capability, including processes, tools, and team structure over time\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Planning, Forecasting \u0026amp;amp; Performance Management\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the annual planning process, long-range planning, and ongoing forecasting cycles for International markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner cross-functionally to develop robust, data-driven forecasts, challenging assumptions and identifying risks and opportunities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive monthly and quarterly business reviews, delivering clear insights into performance drivers and actionable recommendations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure timely and accurate financial reporting, translating results into meaningful business insights for leadership\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Strategic Decision Support \u0026amp;amp; Growth\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead scenario planning and financial modeling to support key business decisions, including market expansion, product launches, and resource allocation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate investment opportunities through ROI analysis, supporting prioritization of high-impact initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Commercial and regional teams to optimize resource deployment and maximize return on investment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support launch planning for new products and geographic expansion, including financial modeling and risk assessment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Pricing, Market Access \u0026amp;amp; Profitability\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with Market Access to support pricing strategy and governance, balancing access considerations with profitability objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct pricing and sensitivity analyses to inform key decisions across markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop a deep understanding of market dynamics, including competitive landscape, reimbursement environments, and access constraints\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and drive margin improvement opportunities through pricing, cost optimization, and strategic trade-offs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Operational Excellence \u0026amp;amp; Process Improvement\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Drive enhancements in financial planning processes, data quality, and reporting capabilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the implementation and optimization of FP\u0026amp;amp;A systems and tools to enable scalable growth\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and standardize best practices across markets while accommodating local market nuances\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Navigate financial complexities across multiple jurisdictions, including FX exposure and evolving market conditions\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Leadership \u0026amp;amp; Stakeholder Management\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Influence and collaborate with senior stakeholders across geographies and functions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present financial insights and recommendations to executive leadership and global finance teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster strong partnerships across International Commercial, ensuring finance is embedded in decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to building a high-performance, collaborative, and accountable culture within the organization\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;12–15+ years of progressive experience in FP\u0026amp;amp;A or finance, with significant exposure to global or international operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience in biotech, pharmaceuticals, or life sciences strongly preferred, particularly in commercial-stage environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience supporting international markets, including product launches and market expansion\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong financial modeling, forecasting, and strategic planning capabilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to influence senior stakeholders and operate as a strategic business partner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in complex, multi-country environments with an understanding of market access and pricing dynamics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to thrive in a fast-paced, high-growth environment with evolving priorities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033156007,"name":"Corporate Functions","child_ids":[],"parent_id":null}],"offices":[{"id":4029419007,"name":"Zug","location":"Zug, Zug, Switzerland","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5138037007","data_compliance":[{"type":"gdpr","requires_consent":true,"requires_processing_consent":true,"requires_retention_consent":true,"retention_period":365,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4632577007,"location":{"name":"Zug"},"metadata":null,"id":5138037007,"updated_at":"2026-06-02T11:27:41-04:00","requisition_id":"2026-MAY-027","title":"Senior Director, International Medical Affairs","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-14T13:57:12-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position reports to the Head of International Medical Affairs and is responsible of conceiving, planning and implementing the medical affairs tactics in the assigned therapeutic area. He/she will also contribute to establish the international medical strategy through cross functional interaction, in alignment with medical leads in the Countries and sitting in the Global medical Affairs Team (GMAT). He/she will lead the scientific initiatives within the European countries that Mirum directly supports and with our distributor partners.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Coordinate the international medical plan development and execution for the assigned area, ensuring consistency with the country level plans and with the GMAT.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the development of scientific symposia at congresses and other medical education initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Plan and execute EU congress related medical activities: KOL engagement, advocacy engagement, scientific booths in alignment with product strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organize and support scientific advisory boards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present scientific data at key congresses and provide input/feedback into final congress presentations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Int Med Affairs in EU PAG engagement/ advocacy; collaborate with and support Int PAG strategy and develop/ execute related tactics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support commercial on various tactics (e.g. EU and Global Brand Plans and commercial training).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support distributors markets on medical strategy, scientific education and contribute to country visits as appropriate\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support externally sponsored research (ESR) and Phase IV studies assessment to ensure strategic alignment and scientific and methodologic robustness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support and collaborate with relevant cross-functional International and local stakeholders such as but not limited to market-access, clinical development/ operations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical Degree, Bachelor’s, Master’s, or Doctorate (i.e. RN, BS/BA, MS/MA, PharmD) level of degree from an accredited university/program.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10+ years of biopharmaceutical experience, with an understanding of the current regulatory and compliance environment for prelaunch and postlaunch initiatives for an investigational asset.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Highly organized individual, who possesses the ability to work in a fast-paced agile environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to interact externally and internally to support global business strategy across assets and launches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to coordinate matrix working groups operating across multiple geographies, roles and backgrounds.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must possess excellent oral and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Team player with a hands-on / can-do mindset\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to interact with and coordinates appropriate scientific and medical activities with internal stakeholders (i.e. commercial, clinical operations, statistics, regulatory, publications, chemistry, manufacturing, controls ‘CMC’ etc.) as they relate to on-going medical affairs projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently with limited supervision and guidance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sound judgment within well-defined practices and policies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage budget for assigned projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical experience/research background or knowledge in one of following areas: liver diseases, metabolic diseases or pediatrics is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in Microsoft OneNote, Teams and Office 365 (proficiency with Microsoft PowerPoint and Excel is essential).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Environment:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;This is a high growth, fast paced organization. The ability to be productive and successful in this work environment is critical.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness and ability to travel domestically and internationally is required; it is anticipated that this will be 40% of work time.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033160007,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4029419007,"name":"Zug","location":"Zug, Zug, Switzerland","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5052439007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4592711007,"location":{"name":"Foster City"},"metadata":null,"id":5052439007,"updated_at":"2026-06-02T19:36:39-04:00","requisition_id":"2026-REP-005","title":"Senior Director, Regulatory Affairs CMC ","company_name":"Mirum Pharmaceuticals","first_published":"2026-02-16T13:16:53-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSTION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Director, Regulatory Affairs CMC is a position requiring a strong leader who will provide strategic and operational leadership, and who will ensure the effectiveness of the Regulatory Affairs CMC team within the Regulatory Affairs department and across the organization. The position will be responsible for all CMC-related submissions: strategic planning, execution, and ensuring quality and accurate supporting documents are submitted within the agreed upon timelines. The ideal candidate will need to be able to accurately interpret and discuss CMC data within cross-functional teams and with Health Authorities.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversees the development and implementation of all regulatory CMC strategies to support market applications, post-marketing CMC commitments, and global development programs across Mirum portfolio.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Directly leads the regulatory CMC strategy for assigned projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for ensuring the appropriate execution of all regulatory CMC strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actively seeks out knowledge of overall corporate planning, business objectives, and current regulatory requirements to develop regulatory positions for assets in Mirum portfolio, and incorporates this knowledge into submission planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensures the effectiveness of the Regulatory CMC team in developing submissions and in working across functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clearly articulates regulatory challenges/risks, identify potential solutions, leads the preparation of risk assessments on regulatory CMC topics, and effectively oversees change controls\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Builds and manages relationships through active partnering with key internal and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensures CMC dossiers meet ICH format and content requirements, as well as specific local requirements of individual countries.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyzes and exercises judgment on complex issues, guided by a thorough understanding of CMC.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports regulatory submissions (NDA, MAA, etc.), Briefing Packages, and response documents for Health Authority interactions and address questions/requests, as well as annual updates (e.g., IB, NDA ARs, IND ARs).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous experience leading CMC discussion during meetings with Health Authorities, and regulatory CMC strategy for small molecule, biologics and orphan/breakthrough programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effectively manages direct report(s) and provides mentorship to junior professionals.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 12 years of relevant experience in Regulatory Affairs CMC.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in drug development focused on market applications (NDA, sNDA, MAA and variations), investigational applications (INDs, CTAs) and commercial lifecycle.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree in a relevant scientific discipline required, PhD in chemistry or other relevant scientific field is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must have experience with small molecules and biologics regulatory CMC activities, late-stage development through commercialization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Combination product experience/knowledge preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated track record of successful submissions to FDA and/or other Health Authorities, including EMA. Regulatory experience/exposure to Japan and China is a plus, and other regions/countries (e.g., Canada, LATAM, MENA, Australia/NZ) is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to apply scientific principles to assess regulatory issues, request and collect relevant information, analyze data, establish facts and draw valid conclusions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal, verbal and written communication skills as well as the ability to effectively partner with and influence others are essential in this collaborative work environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding people management and mentorship skills are required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent planning and organizational skills and ability to work simultaneously on multiple projects with tight timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable in a fast-paced, small company environment with minimal direction and able to adjust workload based upon changing priorities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Environment:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;This is a high-growth, fast-paced organization. The ability to be productive and a team player s critical.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work under minimal supervision.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness and ability to travel domestically and internationally is required. It is anticipated that this will be 5-10% of work time.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $280,000 to $310,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033161007,"name":"Regulatory Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5106256007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4617311007,"location":{"name":"US Remote"},"metadata":null,"id":5106256007,"updated_at":"2026-06-02T19:37:17-04:00","requisition_id":"2026-REP-014","title":"Senior Director, Scientific Affairs - Bone \u0026 Endocrinology","company_name":"Mirum Pharmaceuticals","first_published":"2026-04-13T15:00:59-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The position will lead Scientific Affairs activities that support the overall strategic plan directed towards the diagnosis and management in rare disease. This individual will serve as a genetics and bone and endocrinology expert and support all appropriate activities across the company.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position is field-based requiring engagement with physicians, key opinions leaders in medicine and research, and patient advocacy leaders.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Key activities include:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Leading data generation plans to address evidence gaps in the bone and endocrinology areas.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Driving real-world evidence activities (e.g., phase IV studies, managed access programs, etc.) to inform regulatory, commercial and access requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supporting the analyses and dissemination of data from real-world registries and data repositories for the therapeutic area.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Overseeing secondary analyses of clinical trials data based on field insights and critical knowledge gaps.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contributing to the overall strategic plan and developing data generation and dissemination activities that support the plan\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leading the development of scientific publications that support the overall Brand Plan and Medical Strategic Plan that are directed towards the diagnosis and management of the therapeutic area\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partnering with other functional teams to develop educational materials for different stakeholders (e.g., physicians, patients) that aid in the diagnosis and management of the therapeutic area\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Educating appropriate internal teams on the therapeutic area\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identifies, can gain access to, and develops professional relationships with thought leaders and other healthcare professionals, active and potential study investigators, and professional organizations within their assigned geography\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engages in scientific exchange in response to thought leader requests\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a liaison between HCPs who express interest in conducting investigator-initiated research to facilitate review and consideration of research proposals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborating with external scientists and clinicians on projects related to the diagnosis and management for the therapeutic area\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Utilizes scientific resources to deliver impactful presentations to varying audiences and in a variety of different settings including (but not limited to) advisory boards and patient advocacy groups.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced science or clinical degree at Masters level or above (e.g. MD, DO, Pharm.D., PhD, NP, PA, MPH, MHS, or MS)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 10 years of experience in medical affairs or clinical/scientific research and publications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge in rare disease\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Background in clinical research including experience generating and analyzing data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as author on scientific publications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to write and edit content for scientific abstracts, posters, presentations, digital enhancements, and manuscripts aligned with scientific narrative and objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work collaboratively with external stakeholders and internal cross-functional team.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills, and Abilities:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Understanding of statistical methods in clinical study design, survival and longitudinal analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Background in epidemiology and/or biostatistics to enable the identification of the appropriate analytic strategy to evaluate scientific questions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to analyze data with Excel or equivalent\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding oral and written communication skills with the ability to communicate complex scientific concepts in a compelling and concise manner to various internal and external stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal communication skills, strong personal integrity, adept at networking, and possesses strong oral, written, and communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to identify relevant literature to support scientific publications and strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled in the development and interpretation of data tables and visualizations to support scientific communication\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Well-versed using common tools in scientific publications including collaborative authoring through MS Word, PowerPoint and Excel\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent collaboration skills to be able to work with other internal functions, external collaborators, authors/reviewers to obtain feedback and incorporate information into a final product\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to organize and prioritize tasks in order to maintain deadlines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to travel up to 30%\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-REMOTE\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033160007,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4032948007,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5130723007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4628874007,"location":{"name":"Foster City"},"metadata":null,"id":5130723007,"updated_at":"2026-06-02T19:38:29-04:00","requisition_id":"2026-MAY-030","title":"Senior Director, US Market Access ","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-06T18:19:18-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a rare disease company with a growing portfolio of innovative therapies and a robust pipeline, Mirum is committed to improving the lives of patients who often face limited treatment options and complex care journeys.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We operate with a deep sense of purpose and urgency—grounded in our values: Care. Have Fun. Be Real. Get it Done. As we continue to scale, market access plays a critical role in ensuring that innovation translates into real-world patient access.\u0026amp;nbsp; The Senior Director of U.S. Market Access will:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Shape and elevate U.S. market access strategy to drive optimal coverage, pricing, and patient access across the existing portfolio and future assets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead critical access decisions end-to-end—owning pricing strategy, payer positioning, and execution with a high degree of autonomy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Challenge the status quo by introducing differentiated, insight-driven approaches rooted in real-world payer dynamics and behavior.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;This role is highly cross-functional and enterprise-facing, partnering across Commercial, Medical, Patient Services (HUB), Government Pricing, Legal/Compliance, and Supply Chain to shape and deliver meaningful access strategies. The ideal candidate blends strategic vision with operational experience, bringing deep payer expertise and a passion for rare disease patients.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the development of market access strategies that drive coverage expansion, policy optimization, and quality of access (QOA) improvements across commercial and government payers for inline and pipeline assets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify key differentiators critical to payers for rare disease products in competitive environments and translate into actionable strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Anticipate and shape payer dynamics in rare disease to craft clear, differentiated value narratives that resonate in competitive rare disease markets (UM criteria, specialty pharmacy distribution, generics/biosimilar pressure) for both in-line and pipeline assets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translate clinical and economic evidence into practical, payer-ready tools that influence coverage and reimbursement decisions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead pre-launch payer engagement, value evidence planning, and access readiness to ensure optimal coverage pathways, especially in competitive markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner cross-functionally with medical and marketing to ensure evidence generation is targeted, efficient, and directly aligned to access impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engage directly with payer stakeholders to uncover actionable insights and convert them into strategic access decisions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Align with the US Head of Payer Accounts on strategic account planning and escalation for high-impact access challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as the enterprise voice of access, influencing key decisions across brand strategy, pricing, and commercialization planning workstreams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Government Pricing on policy implications (e.g., Medicaid best price, 340B, IRA/GUARD considerations)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with all regulatory and legal requirements\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; MBA or advanced degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10+ years of experience in market access, payer marketing, or reimbursement, with rare disease experience strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success in launching and optimizing access for specialty/rare disease therapies, including pricing strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Commercial and government payer dynamics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior authorization, appeals, and reimbursement pathways\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;li\u0026gt;Successful experience in leading and developing a team within the market access function \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead cross-functional teams and influence senior leadership in small biotech/rare disease companies with agile working environments a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical, strategic, and communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Resilient and adaptable and proven experience in navigating complex payer dynamics with confidence\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $280,000 to $315,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5133097007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4630104007,"location":{"name":"Foster City"},"metadata":null,"id":5133097007,"updated_at":"2026-06-02T19:39:27-04:00","requisition_id":"2026-MAY-031","title":"Senior Manager, Bioanalytical","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-08T14:31:17-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Manager, Bioanalytical will be responsible for all aspects of bioanalytical in the development and approval of Mirum rare disease assets.\u0026amp;nbsp; As a key member of the small Clinical Pharmacology \u0026amp;amp; Nonclinical Sciences group, the individual will represent these multiple functions on multidisciplinary drug development teams to define the strategy and oversee the execution of required studies/analyses through CROs to achieve team goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serves as the bioanalytical lead on project and study teams, providing subject matter expertise on clinical development programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leads the design and is responsible for the execution of nonclinical and clinical bioanalytical studies for all Mirum assets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manages collaborations with CROs and consultants, providing technical oversight as needed and ensuring timely and quality deliverables to fulfill project goals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leads the completion of the relevant sections of IND, NDA, MAA, other regulatory documents and works closely with Regulatory to support clinical document submission\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides CROs with technical oversight as needed and ensures that assay development, validations, sample analysis, and data transfers occur at CROs and in-house to meet project goals\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS in Biological Sciences and minimum of 6-8 years of relevant experience, or an advanced degree (MS, PhD) with fewer years of experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with assets in liver, neurology, or rare disease indications is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior hands-on laboratory experience operating LC-MS/MS systems (or other quantitative instrumentation) and conducting sample preparation and analysis\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of GLP/GCLP compliance in supporting nonclinical and clinical studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid project management skills: ability to create and manage project plans, budgets, and schedules\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills (written and verbal) and interpersonal skills with an ability to communicate to people at all levels of the organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Functions efficiently, effectively and at times independently\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of success as both an individual contributor and a collaborative team member\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience coordinating studies through CROs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Recognized for being self-directed, well-organized, flexible, and detail-oriented; able to complete multiple activities while maintaining quality\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;The salary range for this position is $200,000 to $220,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033162007,"name":"R\u0026D","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5091877007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4610711007,"location":{"name":"Foster City"},"metadata":null,"id":5091877007,"updated_at":"2026-06-02T19:40:38-04:00","requisition_id":"2026-REP-012","title":"Senior Manager, Clinical Data Management","company_name":"Mirum Pharmaceuticals","first_published":"2026-03-27T15:20:06-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSTION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;The Senior Manager, Clinical Data Management will collaborate primarily with internal team members and external vendors to manage all data collection and data reporting aspects. In addition, the Senior Manager will lead the development of systems and procedures to assure consistency across the Clinical Data Management department. \u0026amp;nbsp;\u0026amp;nbsp;Overall responsibilities will include supporting clinical data management activities from study start-up through study closure in support of trial objectives and corporate goals in accordance with Standard Operating Procedures (SOPs) and regulatory directives. Participate in staff recruitment, onboarding, training and mentoring.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;PRIMARY RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage and monitor the progress of data management activities with CROs or other vendors on assigned studies, build effective relationships with CRO/vendor counterparts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to review and provide feedback to the multi-disciplinary team on other study documents e.g. clinical study protocols, protocol deviation plans, medical monitoring plan, statistical analysis plan, mock Tables, Figures and Listings (TFL) shells and Clinical Study Reports (CSRs)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reviews and approves DM related documentation for quality, completeness, and accuracy; including but not limited to Case Report Forms, Data Validation Specifications, Case Report Form Completion Guidelines, Data Management Plans, Data Transfer Agreements, Medical Coding Guidelines, Validation Plan, User Acceptance Testing (UAT) documentation, Data Review Plan, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track and manage progress towards data deliverables through effective metrics tracking, analysis, and reporting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute procedures for data quality review and data acceptance prior to data analyses and/or database lock\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of standard coding dictionaries MedDRA, WHOdrug, etc., and related best practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attends and represents CDM effectively on all assigned studies and programs at relevant meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understand critical tasks and milestones; ensure data management deliverables are met per study timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the clinical study budget, ensuring the project remains within scope through reviewing and approving invoices, identifying out-of-scope activities and its appropriate handling\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work collaboratively with biostatistics, programming and other functions to meet project deliverables and timelines for clinical data acquisition, quality checking and reporting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor in-house resources of assigned projects and identify potential deficiencies; work with supervisor to develop and implement a plan to overcome any obstacles\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to developing and implementing departmental policies, standards and process improvement initiatives as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support implementation of data standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Align with and support management and corporate goals or objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to activities supporting audits \u0026amp;amp; inspection readiness and regulatory inspections\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in selecting vendors/CROs e.g. reviewing RFIs/RFPs and participating in bid defenses\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify, manage, mentor and develop Clinical Data Management team members\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Good working knowledge of medical/scientific terminology and knowledge of ICH guidelines and regulations relating to data management activities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s Degree preferably in a scientific or health-related discipline; Master’s degree is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8+ years of clinical data management experience in a pharmaceutical/biotech setting\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to prioritize and manage multiple tasks with conflicting deadlines in support of corporate goals and objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in managing outsourced clinical data management activities and/or other vendors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thorough understanding of the drug development process, clinical trial methodology, regulatory requirements, ICH, GCP and GCDMP\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Current and extensive knowledge of industry CDM best practices and processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong experience with various clinical database management systems including EDC, eCOA, and ePRO\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong and effective oral and written communication, project management, and interpersonal skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success working in a virtual, global and multi-cultural environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success in identifying creative solutions to complex study-related or technical issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of SAS, EDC programming, systems integration experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of CDASH and CDISC standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to mentor junior staff\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $185,000 to $205,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033162007,"name":"R\u0026D","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5126426007","data_compliance":[{"type":"gdpr","requires_consent":true,"requires_processing_consent":true,"requires_retention_consent":true,"retention_period":365,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4626953007,"location":{"name":"Zug"},"metadata":null,"id":5126426007,"updated_at":"2026-05-11T15:19:17-04:00","requisition_id":"2026-REP-015","title":"Senior Manager, International Accounting ","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-01T14:46:59-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Manager, International Accounting, will be a key member of the accounting team within a publicly traded biotechnology company. This role is responsible for overseeing the day-to-day accounting operations of foreign subsidiaries and supporting the company’s expanding global presence by ensuring the accuracy and integrity of international financial data. The position requires a strong understanding of statutory reporting, payroll accounting, revenue recognition, accrual processes, intercompany transactions, and full balance sheet reconciliations. The ideal candidate will bring solid technical accounting expertise, sound professional judgment, and experience operating within a SOX 404(b)-compliant environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;Manage accounting functions across multiple jurisdictions, including the monthly and quarterly close process (execution and review of journal entries, reconciliations, and variance/flux analysis).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;Own end-to-end revenue recognition in accordance with ASC 606, including monthly reporting, journal entries, and liaison with 3PL providers to validate sales and accounts receivable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with third-party providers (payroll, tax, legal and compliance) to ensure timely and accurate information for payroll processing and VAT, corporate tax filings, in line with local regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute monthly accrual processes in collaboration with business partners, FP\u0026amp;amp;A, and PO owners, ensuring estimates are accurate and appropriately supported\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate statutory audits for foreign entities, ensuring timely delivery of documentation and strict compliance with local filing timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support consolidated U.S. GAAP financial statement audits by preparing detailed schedules and addressing auditor queries for assigned areas\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support accounting operations for foreign subsidiaries, including procure pay, cost of goods sold, inventory accounting, and intercompany cross-charges in accordance with established policies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with flux analyses to ensure results are accurate and prepared in accordance with US GAAP guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and document key accounting processes and internal controls to ensure full compliance with SOX requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify opportunities to improve efficiency and standardize accounting processes, including through automation, and support process optimization initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in system improvements, ad hoc analyses, and special projects as assigned to support operational efficiency and strategic initiatives\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education /Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s or Master’s degree in accounting or finance; relevant professional certifications (e.g., CPA or international equivalents) an added advantage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5–7 years of experience in accounting and financial reporting, including public accounting experience (e.g., EY, Deloitte, or similar)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of U.S. GAAP and international accounting, preferably within a publicly traded biotech or life sciences company\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of accounting for foreign subsidiaries and consolidations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience managing general ledger functions, with proficiency in accounting systems such as NetSuite or similar experience with NetSuite (Multi book, OneWorld/Consolidation modules) and foreign currency reporting is a plus)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical skills, attention to detail, and ability to meet tight deadlines.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;A sense of ownership and pride in your performance and its impact on the company’s success\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Positive, self-confident and decisive work ethic with excellent communication skills in both oral and written formats, as well as excellent listening skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated and self-managed - able to think independently and creatively\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to build and scale processes with strong analytical skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of internal controls and SOX compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Energy to commit to a fast-paced environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be detail oriented yet not lost in the details\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A team player and able to support other departments to achieve objectives\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033156007,"name":"Corporate Functions","child_ids":[],"parent_id":null}],"offices":[{"id":4029419007,"name":"Zug","location":"Zug, Zug, Switzerland","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5138289007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4632697007,"location":{"name":"Foster City"},"metadata":null,"id":5138289007,"updated_at":"2026-06-02T19:46:55-04:00","requisition_id":"2026-REP-020","title":"Senior Product Manager, LIVMARLI Marketing ","company_name":"Mirum Pharmaceuticals","first_published":"2026-05-20T16:18:44-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Product Manager, Patient Marketing for LIVMARLI, will play a critical support role to the Senior Marketing Director in the strategic and tactical execution of marketing initiatives to support the continued success of LIVMARLI. This individual will help plan, coordinate, and implement key brand activities across digital, field, patient, and healthcare provider channels.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is ideal for a motivated, resourceful, and digitally-savvy professional who is eager to learn, take ownership of meaningful projects, and grow within a high-performing, mission-driven commercial team.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Brand \u0026amp;amp; Marketing Support\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with the Senior Director, Marketing to execute the annual brand plans for LIVMARLI.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in developing marketing materials (Patient/caregiver, digital, etc.) in alignment with strategic objectives and compliance standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support execution of omnichannel marketing initiatives, including HCP and patient campaigns, digital content, CRM/email marketing, and social media.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate review and approval (MLR) processes, ensuring materials are accurate, timely, and compliant.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support tactical execution of field force tools and branded and unbranded education initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage creative and digital agency partners, ensuring deliverables are high-quality, compliant, and on-time.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support ongoing field team enablement through tools, resources, and internal communications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain awareness of emerging digital tools and rare disease engagement innovations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help maintain brand budgets and timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare summaries, presentations, and reports for leadership and brand review meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with cross-functional partners (Medical Affairs, Market Access, Patient Services, Commercial Operations, and Field Teams) to ensure alignment and seamless execution.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education \u0026amp;amp; Experience\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in business, marketing, life sciences, or related field required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3–6 years of experience in pharmaceutical marketing, product management, or commercial operations, ideally in rare disease.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational, project management, and communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High attention to detail with ability to manage multiple priorities and deadlines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Digital fluency – comfortable with CRM systems, analytics platforms, and digital campaign tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analytical mindset – able to synthesize data and insights to inform decisions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $175,000 to $185,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5087346007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4608789007,"location":{"name":"Foster City"},"metadata":null,"id":5087346007,"updated_at":"2026-06-02T19:44:20-04:00","requisition_id":"2026-BUD-007","title":"Senior Specialist, Clinical Supply Chain","company_name":"Mirum Pharmaceuticals","first_published":"2026-03-23T16:45:53-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSTION SUMMARY\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Reporting to the Executive Director, Clinical Supply Chain, the Senior Specialist is responsible for supporting the senior team members in managing the global supply and distribution of investigational drug product for Mirum’s ongoing clinical trials inclusive of the oversight management of multiple Contract Manufacturing Organizations (CMOs) and distribution providers. The ideal candidate is a detailed oriented, self-starter, proactive, with the ability to work independently under minimal supervision.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Supports the development and execution of Clinical Supply strategies for all Mirum investigational drug products in collaboration with senior team members.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists in creating and maintaining the Clinical Supply forecasting models to ensure investigational material production aligns with corporate and financial goals, study enrollment, and business continuity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports Clinical Supply program activities for investigational drug product inventory management and distribution in partnership with CMOs; evaluates drug utilization versus forecast considering country requirements and logistical timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides support for the oversight of Clinical Supply CMOs, including assisting in selection (RFI), contract negotiations, financial review, daily operations, and routine assessment of CMO performance via formal Business Reviews.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists with the management of global resupply strategies in IRT systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interacts with the Clinical Operations, CMC, Quality, and other functions to ensure optimal execution of the Clinical Supply strategy for investigational drug products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports project-related interactions with IRT vendors and Contract Research Organizations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains study and depot-level accountability and reconciliation documentation to support regulatory compliance and study closeout.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Archives documentation on Trial Master Files as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Archives Proof of Delivery (POD) documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for the creation, periodic review, and maintenance of all Clinical Supply SOPs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accountable for initiating, overseeing, and resolving departmental deviations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tracks and resolves temperature excursions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports the preparation and review of Mirum documentation including regulatory applications, clinical trial applications, routine amendments, protocols, briefing documents, Quality Technical Agreements, responses to health authority inquiries, and other documents as required.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Degree in biological or life sciences, pharmacy or medicine (or international equivalent). A minimum of 5 years in the pharmaceutical industry or relevant work experience and a minimum of 3 years in Clinical Supply Chain.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiar in the daily management and operations of a Clinical Supply Chain inclusive of bulk management, distribution, and maintaining study blinds across multiple investigational products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experienced with Clinical Supply Chain systems for inventory management and resupply (Interactive Response Technology – IRT).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent planning and organizational skills and the ability to work simultaneously on multiple projects with tight timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication skills both in writing and verbally.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assisting as the Clinical Supply Chain support during Regulatory Inspections and Audits.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experienced with Clinical Supply Chain systems for inventory management and resupply (Interactive Response Technology – IRT).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of import / export requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive in supporting cross-functional collaboration and team performance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Good knowledge of industry technology.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Applies and drives Forecasting and Planning activity as it relates to protocol.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to build/drive internal team consensus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translates broad strategies into specific objectives and action plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiar with team and individual leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge and experience relating to clinical trials would be desirable.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $115,000 to $125,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033157007,"name":"Supply Chain","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5016170007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4575484007,"location":{"name":"Foster City"},"metadata":null,"id":5016170007,"updated_at":"2026-06-02T19:46:06-04:00","requisition_id":"2026-REP-001","title":"Vice President, Clinical Pharmacology","company_name":"Mirum Pharmaceuticals","first_published":"2026-01-06T17:56:53-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Executive leader responsible for Clinical Pharmacology strategy and its integration across all development programs at Mirum, with potential scope to oversee broader pharmacology functions, including nonclinical pharmacology, depending on candidate experience.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the design and execution of a clinical pharmacology development plan for all Mirum assets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Set the clinical pharmacology strategy across the portfolio aligned with corporate and regulatory objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop resource plans via employees and vendors to enable clinical pharmacology development of Mirum assets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and lead the Clinical Pharmacology function, including talent strategy and capability development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and influence cross-functional teams to achieve clinical pharmacology goals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a key contributor to development governance and decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Continually review and monitor guidance, regulations, and publications in clinical pharmacology development and relevant therapeutic areas\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide input on clinical safety programs (informed consent, exclusion criteria, pregnancy, etc.) and clinical pharmacology programs (ADME, DDIs, PK/PD, BE, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and work with expert consultants as needed to fill project needs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure completion of relevant sections of IND, NDA, MAA, and other regulatory documents, and ensure robust responses to information requests\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a senior representative with regulatory agencies, including responses to queries, preparation of pre-meeting documents, and participation in Health Authority meetings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead due diligence efforts for potential drug in-licensing or partner opportunities, including assessment and review of existing data and development of clinical pharmacology strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Scope may expand to include leadership of nonclinical pharmacology activities, aligned with candidate expertise and organizational needs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced science degree (e.g. PhD, PharmD)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10+ years leadership experience and 15+ years drug development experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ability to understand and effectively communicate scientific information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thorough understanding of the nonclinical and clinical pharmacology requirements, including regulatory guidance, to support drug development in US and EU\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep knowledge of pharmacodynamics and pharmacokinetics principles and modeling\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience coordinating studies through CROs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience authoring and supporting regulatory filings (INDs, NDAs, MAA, DSURs, IBs, etc)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The salary range for this position is $320,000 to $340,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033162007,"name":"R\u0026D","child_ids":[],"parent_id":null}],"offices":[{"id":4029418007,"name":"Foster City HQ","location":"Foster City, California, United States","child_ids":[4034605007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5068517007","data_compliance":[{"type":"gdpr","requires_consent":true,"requires_processing_consent":true,"requires_retention_consent":true,"retention_period":365,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4600245007,"location":{"name":"Zug"},"metadata":null,"id":5068517007,"updated_at":"2026-05-31T23:43:16-04:00","requisition_id":"2026-REP-009","title":"Vice President, Commercial Operations International","company_name":"Mirum Pharmaceuticals","first_published":"2026-03-03T17:44:02-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSTION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Aa core member of the International Leadership, this position plays a key strategic and operational role within International Region. The Vice President Commercial Operations will lead International Regions in all aspects of commercialization and business performance: strategy, brand planning process, tactical execution, launch readiness and execution, operational excellence and delivering on established KPIs. This position will be key in driving the commercialization of the company’s existing portfolio and upcoming launches. The individual will work closely with cross-functional team across the organization.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute the International commercial strategy in alignment with global priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead end-to-end launch excellence across International markets, including readiness planning, resource allocation, market sequencing, and post-launch performance optimization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help build the Mirum culture by serving as an effective bridge between International and US teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure execution of all operational business activities to maximize patient access and commercial impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead regional marketing and commercial operations team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure the critical linkage across commercial, medical affairs, regulatory affairs, market access, finances, compliance and to support all partners in executing best in-class operational activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Continuously assess productivity and efficiency of commercial organization, lead commercial operating model strategic thinking across markets – directly or in close collaboration with partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive initiatives to prepare for further sustainable growth in International: commercial KPIs benchmarking, business plan, sales plans and forecasting models, marketing tactics, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prioritize key strategic initiatives in collaboration with global / International leadership team and other stakeholders to build optimal organization that enables long term sustainable growth.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner for all global Business development opportunities assessment in the region.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure adherence to all relevant legal, regulatory and compliance requirements, corporate policies and procedures.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Extensive expertise in the pharmaceutical/biotech commercial operations, in multiple healthcare systems, especially in European markets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven successful experience in operational commercial role at regional as well as local country level.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on involvement in the development of commercial strategy, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Rare or ultra-rare disease experience preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Good understanding of commercial, access and regulatory process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Undergraduate degree required, MBA and/or relevant postgraduate qualifications preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;15+ years experience in life sciences, start up, biotech or pharma industry, in marketing/commercial functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Eligibility to work in Switzerland (valid Swiss work permit) is required.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong strategic thinking and capacity to execute strategy in a variety of business environment in International region.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to drive initiatives and lead new projects in a lean organization by working cross functionally and using key stakeholders’ areas of expertise.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Enjoy building and creating and is a self-starter.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly organized and comfortable managing multiple work streams at once.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional communication and interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Great attention to detail and self-motivation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to travel internationally\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-HYBRID\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4029419007,"name":"Zug","location":"Zug, Zug, Switzerland","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5158059007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4642348007,"location":{"name":"US Remote"},"metadata":null,"id":5158059007,"updated_at":"2026-06-06T11:38:07-04:00","requisition_id":"2026-TBD-001","title":"Zone Director, East","company_name":"Mirum Pharmaceuticals","first_published":"2026-06-06T11:36:22-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The \u0026lt;strong\u0026gt;Zone Director\u0026lt;/strong\u0026gt; is a second-line field leader responsible for driving commercial performance, building 4 high-performing Region Business Director (RBD) teams, and ensuring execution excellence across the liver portfolio. This role translates national strategy into regional impact, with a strong emphasis on rare disease expertise, patient-centricity, and cross-functional leadership.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Assigned Area: ME, NH, VT, NY, RI, MA, CT, NJ, PA, DE, MD, D.C., VA, OH, MI, IN, TN, NC, SC,\u0026amp;nbsp;GA, FL\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Enterprise Leadership\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own and deliver Zone business performance across the liver portfolio with a strategic, big-picture mindset\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive change and innovation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute zone-specific business plans aligned to national strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze market trends, competitive dynamics, and performance data to inform actions\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Team Leadership \u0026amp;amp; Development\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead, coach, and develop first-line leaders to maximize team effectiveness\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build a strong leadership pipeline and succession plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster a culture of accountability, engagement, and continuous improvement\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Execution Excellence\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure consistent and high-quality execution of brand strategy in the field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor KPIs and drive disciplined performance management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and scale best practices across regions\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Cross-Functional Collaboration\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with Marketing, Market Access, Medical Affairs, Patient Services and Operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure alignment on strategy and coordinated execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide field insights to inform brand planning and lifecycle strategy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Market \u0026amp;amp; Customer Engagement\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain strategic relationships with key opinion leaders (KOLs) and top accounts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understand regional nuances in referral patterns and treatment pathways\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support teams in navigating complex access and reimbursement environments\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Compliance \u0026amp;amp; Ethical Leadership\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure all activities comply with regulatory, legal, and company policies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Model integrity and patient-first decision making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reinforce a culture of compliance across the organization\u0026amp;nbsp;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; advanced degree preferred (MBA, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;7+ years pharmaceutical/biotech experience, plus minimum of 5 years of leadership experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Successful experience leading leaders (second-line leadership) highly desired\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Significant rare disease and/or specialty experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in rare liver disease a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success in product launches, ideally with first-in-class therapies and in competitive markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to build, lead, train and develop high-performing teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success in sales leadership roles with the ability to inspire, influence and align teams\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience navigating complex rare disease patient journeys, including diagnosis, referral pathways, and difficult access to therapies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong leadership presence with the ability to inspire, influence, and align teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of market access, payer dynamics, and patient services\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead in a matrixed organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High integrity, ethical standards, and commitment to compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thrives in a fast-paced, dynamic, and collaborative environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to travel frequently, up to 70% overnight travel and has a valid drivers’ license\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-REMOTE\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4032948007,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5158040007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4642340007,"location":{"name":"US Remote"},"metadata":null,"id":5158040007,"updated_at":"2026-06-06T11:37:42-04:00","requisition_id":"2026-TBD-002","title":"Zone Director, West","company_name":"Mirum Pharmaceuticals","first_published":"2026-06-06T11:37:42-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MISSION\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The \u0026lt;strong\u0026gt;Zone Director\u0026lt;/strong\u0026gt; is a second-line field leader responsible for driving commercial performance, building 4 high-performing Region Business Director (RBD) teams, and ensuring execution excellence across the liver portfolio. This role translates national strategy into regional impact, with a strong emphasis on rare disease expertise, patient-centricity, and cross-functional leadership.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Assigned Area: WA, OR, CA, NV, AZ, UT, ID MT, WY, CO, NM, TX, KS, SD, ND, OK. LA, AR, MO, IA, MN, WI, IL, KY, MS, AL\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;JOB FUNCTIONS/RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Enterprise Leadership\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own and deliver Zone business performance across the liver portfolio with a strategic, big-picture mindset\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive change and innovation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute zone-specific business plans aligned to national strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze market trends, competitive dynamics, and performance data to inform actions\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Team Leadership \u0026amp;amp; Development\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead, coach, and develop first-line leaders to maximize team effectiveness\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build a strong leadership pipeline and succession plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster a culture of accountability, engagement, and continuous improvement\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Execution Excellence\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure consistent and high-quality execution of brand strategy in the field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor KPIs and drive disciplined performance management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and scale best practices across regions\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Cross-Functional Collaboration\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with Marketing, Market Access, Medical Affairs, Patient Services and Operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure alignment on strategy and coordinated execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide field insights to inform brand planning and lifecycle strategy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Market \u0026amp;amp; Customer Engagement\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain strategic relationships with key opinion leaders (KOLs) and top accounts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understand regional nuances in referral patterns and treatment pathways\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support teams in navigating complex access and reimbursement environments\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Compliance \u0026amp;amp; Ethical Leadership\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure all activities comply with regulatory, legal, and company policies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Model integrity and patient-first decision making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reinforce a culture of compliance across the organization\u0026amp;nbsp;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education/Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; advanced degree preferred (MBA, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;7+ years pharmaceutical/biotech experience, plus minimum of 5 years of leadership experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Successful experience leading leaders (second-line leadership) highly desired\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Significant rare disease and/or specialty experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in rare liver disease a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success in product launches, ideally with first-in-class therapies and in competitive markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to build, lead, train and develop high-performing teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success in sales leadership roles with the ability to inspire, influence and align teams\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience navigating complex rare disease patient journeys, including diagnosis, referral pathways, and difficult access to therapies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong leadership presence with the ability to inspire, influence, and align teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of market access, payer dynamics, and patient services\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead in a matrixed organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High integrity, ethical standards, and commitment to compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thrives in a fast-paced, dynamic, and collaborative environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to travel frequently, up to 70% overnight travel and has a valid drivers’ license\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;#LI-REMOTE\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4033158007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4032948007,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]}],"meta":{"total":43}}