{"jobs":[{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7619279003#open-positions","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":5713865003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7619279003,"updated_at":"2026-03-19T11:20:21-04:00","requisition_id":"2642","title":"Associate Director, Clinical Data Management","company_name":"Kymera Therapeutics","first_published":"2026-02-04T15:08:45-05:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Act as Lead Data Manager, overseeing all deliverables of activities outsourced to DM CRO for multiple studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact and manage relationships with other functional areas to ensure high quality data management activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversight of data collection tools (EDC, DTAs, EDC integrations) and essential documents (DMP, UAT Documents, data edit specifications, annotated case books and data entry guidelines)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in User Acceptance Testing Activities for the applicable Data Collection Tools\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform Quality Control for the data completeness and accuracy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in and support data cleaning, query generation and resolution and review of medical coding as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for adhering to the Data Management timelines and budget.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide technical expertise to help in the use of technologies for Data Management and the clinical study team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the development of lessons learned and best practices as well as help develop SOPs and internal working procedures and process improvement initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the establishment of systems and tools to help ensure clinical data security and integrity.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;8+ years’ experience in clinical data management in biotechnology or pharmaceutical industry, with outsourced CRO oversight experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5+ years managing vendor relationships/partnerships in a global environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must have advanced knowledge of Data Management processes and systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of CDISC standards required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Data Visualization Tool experience preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using standardized medical terminology, including but not limited to MedDRA and WHODrug.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal, communication, and organizational skills with the ability to work independently and in a study team environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $145,000 – $215,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057515003,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7726500003#open-positions","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":5761145003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7726500003,"updated_at":"2026-05-15T13:42:37-04:00","requisition_id":"2689","title":"Associate Director or Director, Clinical Operations","company_name":"Kymera Therapeutics","first_published":"2026-05-06T14:40:08-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the planning, implementation, and execution of global clinical trials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Plan, execute, and lead study-specific meetings (e.g., internal core team meetings, investigator meetings, etc), as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide input for the design of the Informed Consent Form(s), eCRFs, monitoring conventions, edit checks, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide study-specific training and leadership to clinical research staff, CRO, CRAs, sites and other contract personnel.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage study timelines and metrics to ensure completion of study deliverables.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead site feasibility and selection qualification, initiation, and oversight of outsourced monitoring activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review monitoring reports to ensure quality and resolution of site-related issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure timely enrollment and data collection at clinical trial sites.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with the data management team to ensure data integrity and timely database lock.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure tracking, review of protocol deviations, and assess impact on study data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with translational medicine team to ensure appropriate incorporation of bioanalytical sampling plan into clinical protocols\u0026amp;nbsp;\u0026lt;u\u0026gt;and\u0026lt;/u\u0026gt; relevant data output of the trial is provided to functional groups for review.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Operational Excellence and assigned Site Engagement Leads to help drive site engagement and bolster recruitment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as key counterpart of Clinical Outsourcing to build RFPs and support the selection of clinical vendors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee and contribute to Sponsor Oversight activities including but not limited to review of KPIs, KRIs, PDs, risks, Data Review Findings, etc. to assess the health of the study and proactively ensure mitigations are in place to achieve Kymera’s quality standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to clinical operations process improvement initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate and complete trial documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify and resolve clinical project issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This role may require up to 25% travel\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS degree and 8+ years of experience in clinical operations in biotech/pharma. 5 years’ experience leading global clinical trials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Inspection readiness experience preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working on large, global, complex phase 2b/3 or late stage trials. Respiratory or Immunology experience highly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Broad knowledge of Global regulations and guidelines including CFR, ICH GCP, HIPAA, GDPR, and the Protection of Human Research Subjects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management skills with the ability to manage multiple trials simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent problem-solving, leadership, and communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in a fast-paced, dynamic environment with cross-functional teams.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $160,000 – $275,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057515003,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7586362003#open-positions","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":5699834003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7586362003,"updated_at":"2026-04-10T13:42:26-04:00","requisition_id":"2621","title":"Associate Director, Product Quality","company_name":"Kymera Therapeutics","first_published":"2026-04-10T13:42:26-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director will act as a Quality subject matter expert for Good Manufacturing Practices (GMP) activities. The individual will be responsible for material disposition; will provide Quality oversight for technical transfers, stability assessments, manufacturing, analytical and distribution activities performed at external suppliers. In addition, the individual will ensure compliance with regulations and Kymera policies and procedures.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide quality oversight of contract organizations associated with the manufacturing and distribution of Drug Substances, Drug Products, and Finished Goods.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with manufacturing and distribution colleagues to (i) review manufacturing batch records, protocols, reports, and specifications, and (ii) perform disposition of critical intermediates, drug substances/drug products, and finished goods.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with CMC analytical colleagues to (i) review test methods, SOPs, analytical data summaries, validation and stability protocols, and technical reports (ii) oversee specification control and shelf life management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure that product quality-related issues, including deviations/OOSs/OOTs and product complaints, are appropriately investigated and resolved.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate cross-functionally and develop strong relationships with internal and external partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the preparation and review of regulatory filing submissions (IND/IMPD/NDA)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help develop and implement phase-appropriate SOPs and policies. Ensure compliance with relevant regulatory requirements such as FDA, EMA, and ICH guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the qualification and performance monitoring of external GMP suppliers and maintain Quality Agreements with them.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and track quality metrics to measure performance and identify trends.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present quality assessments to the Material Review Board and Quality Management Review Board.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide support for late-stage manufacturing and commercialization readiness activities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;8 + years of experience in pharmaceutical manufacturing or laboratory settings, including at least 4 years in a GMP quality assurance role. Experience in a small-molecule manufacturing environment is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience providing Quality oversight of outsourced late-phase GMP manufacturing activities, including process validation and commercial readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in a CMC team setting as a Quality representative.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently and manage multiple projects within the established timelines and objectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong problem-solving ability to evaluate quality matters and make risk-based decisions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $160,000 – $240,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057516003,"name":"Technical Operations \u0026 Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7726507003#open-positions","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":5761147003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7726507003,"updated_at":"2026-05-07T14:31:52-04:00","requisition_id":"2687","title":"Clinical Trial Manager ","company_name":"Kymera Therapeutics","first_published":"2026-05-06T14:45:53-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the planning, implementation and execution of a global clinical trial\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for management of vendors to support clinical trial execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Plan, execute, and lead study-specific meetings (e.g., internal core team meetings, investigator meetings, etc), as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide input for the design of the Informed Consent Form(s), eCRFs, monitoring conventions, edit checks, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide study-specific training and leadership to clinical research staff, CRO, CRAs, sites and other contract personnel.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage study timelines and metrics to ensure completion of study deliverables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support site selection, qualification, initiation, and monitoring activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review monitoring reports to ensure quality and resolution of site-related issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure timely enrollment and data collection at clinical trial sites.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with the data management team to ensure data integrity and timely database lock.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and analyze clinical trial data to identify trends and potential issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure tracking and review of protocol deviations and assess impact on study data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop relationships with investigators and site staff\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with CRO and Medical Monitor to ensure safety and efficacy data appropriately summarized to facilitate review.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with translational medicine team to ensure appropriate incorporation of bioanalytical sampling plan into clinical protocols\u0026amp;nbsp;\u0026lt;u\u0026gt;and\u0026lt;/u\u0026gt; relevant data output of the trial is provided to functional groups for review.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate and complete trial documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify and resolve clinical project issues\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor of Science in Life Sciences and 3+ years (CTM)/5+ years (Sr. CTM) as a project/clinical trial manager in biotech/pharmaceutical industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working on large, global, complex Phase 2 clinical trial(s).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Broad knowledge of regulatory and ICH GCP guidelines, HIPAA, Protection of Human Research Subjects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management skills with the ability to manage multiple trials simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent problem-solving, leadership, and communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in a fast-paced, dynamic environment with cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $115,000 – $200,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057515003,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7763102003#open-positions","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":5776918003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7763102003,"updated_at":"2026-06-04T18:51:37-04:00","requisition_id":"2699B","title":"Data Engineer or Senior Data Engineer, Research Informatics","company_name":"Kymera Therapeutics","first_published":"2026-06-03T17:19:00-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;We\u0026#39;re looking for a technically strong, execution-driven informatics data engineer to serve as the primary technical partner for our Research and Discovery teams. This is a hands-on role for someone who thrives under shifting priorities, moves with urgency, and brings structure to complex, fast-moving scientific environments. You\u0026#39;ll work directly with scientists, CROs, vendors, and IT to build and maintain the data workflows, integrations, and systems that keep research moving.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as a technical informatics contact supporting Research teams across scientific applications, data engineering, data standardization, scientific workflows, and operational informatics activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support cloud-based research infrastructure and contribute to data architecture, metadata standards, and FAIR data practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design, develop, and maintain data pipelines, automations, and integrations across research platforms and external systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Administer, configure, and troubleshoot scientific applications including CDD Vault, D360, Spotfire, Benchling, and related tools\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner directly with Biology and PSLD scientists to identify pain points and deliver scalable informatics solutions — quickly\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage and govern scientific data from internal teams, CROs, and external collaborators, ensuring quality and consistency\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive system implementations, upgrades, and vendor evaluations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create and maintain SOPs, technical documentation, and user training materials\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Required\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Master\u0026#39;s degree or higher in Bioinformatics, Computational Biology, Computer Science, Data Science, Chemistry, Biology, or related STEM field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Data Engineer: 5+ years | Senior Data Engineer: 8+ years of relevant industry experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with research platforms such as CDD Vault, D360, Spotfire, and/or Benchling\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong Python, R and SQL development skills with a track record of building production-grade scientific tools and automations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong experience with scientific data engineering, ETL workflows, APIs, and system integrations across diverse research data types including invitro assay, PK/PD, proteomics, and structural biology datasets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated track record of delivering high-quality work in a fast-paced environment, effectively managing competing priorities with urgency, strong attention to detail, consistent follow-through, organizational excellence, and adaptability to changing business needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to partner effectively with scientists, vendors, and CROs in a research setting\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;AWS cloud services and cloud-native data workflows\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cheminformatics or bioinformatics domain knowledge\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with FAIR data principles and research data lifecycle management\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $115,000 – $215,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4003322003,"name":"G\u0026A","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7653638003#open-positions","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":5727514003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7653638003,"updated_at":"2026-03-05T09:22:00-05:00","requisition_id":"2649","title":"Director, Clinical Data and Systems","company_name":"Kymera Therapeutics","first_published":"2026-03-05T09:22:00-05:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as clinical study team Subject Matter Expert for eCOA, IRT, Data Visualization and other clinical data systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead clinical technologies including planning, execution, and delivery of the clinical data activities on eCOA, IRT and other clinical technologies, implementing standard procedures to initiate best practices and lead data management flow.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the establishment of an overall clinical systems roadmap.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partners with cross-functional team members (e.g., Clinical Operations, Clinical Science, Clinical Data Management, Tech Ops/Clin Supplies, QA, IT, Procurement) to gather relevant study requirements to create the system design, provide subject matter expertise, and ensure expert and on-time system delivery and implementation as well as data quality standards are met.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for user acceptance testing oversight and documentation, including UAT test case creation, facilitating signatures on documentation, and study risk and impact assessments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee data imports and integrations from multiple systems and ensure quality.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for facilitation of clinical system technical support, data changes, data issue resolution; working with cross-functional stakeholders including Clinical Data Management, IT, Clinical Operations and Biostatistics in order to achieve goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and improve data collection processes; partner to identify how to standardize data across multiple systems; provide recommendations for enriched reporting and data standards; support standardization of internal data infrastructure.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;As Business Owner, ensure processes, tools, documents, and training materials related to clinical systems are developed and implemented, as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as technical SME for contracting and budget management activities including establishing initial Scope of Work (SOW) and Change Orders in partnership with Strategic Sourcing, as applicable.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;10+ years of progressive experience in a Systems Management role with a Sponsor/CRO company is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently with a high level of attention and act with initiative to address issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience overseeing IRT/RTSM and eCOA/ePRO systems is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with user requirement specifications/user test scripts with clinical data systems is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience authoring/reviewing procedures (SOPs, WIs) in a GCP environment is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in clinical trial conduct. Hands-on Data Management experience of EDC, eCOA and IRT.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effectively negotiates and influences to solve high impact challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong leadership and project management skills, and is able demonstrate flexibility and agility working within a multi-functional, global matrix.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must have excellent communication skills (verbal and written), and good interpersonal/group skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $195,000 – $275,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057515003,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7479492003#open-positions","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":5658276003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7479492003,"updated_at":"2026-05-13T09:54:45-04:00","requisition_id":"25X46","title":"Director, Clinical Operational Excellence","company_name":"Kymera Therapeutics","first_published":"2025-09-26T13:33:40-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Define and implement the long-term vision for Clinical Operations Excellence, ensuring alignment with corporate objectives and regulatory standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with senior leaders in Clinical Development, Quality, Regulatory, and other functions to harmonize processes and elevate trial execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the design and deployment of scalable, standardized processes, tools, and KPIs across clinical operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee operational performance dashboards, risk management frameworks, and trial health reporting to ensure proactive issue identification and resolution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Champion continuous improvement initiatives that enhance trial efficiency, cost-effectiveness, and speed-to-market.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Quality Assurance to ensure inspection readiness and adherence to compliance frameworks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement frameworks to ensure adherence to regulatory requirements and Good Clinical Practice (GCP) guidelines. Ensure adherence to global regulatory requirements, ICH-GCP, and company SOPs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop training programs and support change management initiatives to embed best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive continuous process improvements to enhance operational efficiency, quality, and effectiveness in clinical oversight.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;10+ years of experience in the biotech/pharmaceutical industry with direct experience in project management within Clinical Operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record in process improvement, clinical trial execution, and operational strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with planning, management, and oversight of activities and deliverables within Clinical Operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of clinical trial management, ICH-GCP, and regulatory compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of managing multiple projects and/or programs concurrently\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent analytical, problem-solving, and organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication and interpersonal skills with the ability to influence cross-functional stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead change and foster a culture of continuous improvement.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $195,000 – $275,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057515003,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7742050003#open-positions","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":5769179003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7742050003,"updated_at":"2026-05-20T15:30:48-04:00","requisition_id":"2696B","title":"Director, Medicinal Chemistry","company_name":"Kymera Therapeutics","first_published":"2026-05-20T15:30:48-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;Who we are:\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;How we work:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;How you’ll contribute:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Drive state-of-the-art multi-parameter medicinal chemistry optimization with creativity, innovation, in-depth analysis of data, and existing literature information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute in a very impactful manner to compound design and synthetic route identification for all portfolio projects\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead medicinal chemistry efforts on validating targets at early stage to clear decision point\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Holistic approach to hit/lead finding including use of structure-based drug design and fragment-based drug discovery\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective leadership and management of CRO chemistry teams through excellent synthetic and medicinal chemistry skills with clear and open communication\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead medicinal chemistry efforts and contribute beyond med chem as part of a multi-disciplinary project team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent the company effectively in scientific matters to external organizations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide mentorship, guidance, and development for junior project leaders and medicinal chemists.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;h3\u0026gt;Skills and experience you’ll bring:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD in organic/medicinal chemistry with 8+ years of experience as a medicinal chemist/project leader in the biotech/pharmaceutical industry with a track-record of leading/contributing to research projects towards IND-track nomination\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive knowledge of modern medicinal chemistry strategies for the optimization of DMPK, biochemical, pharmacological and safety\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent synthetic organic chemistry skills and creativity are required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability as chemistry leader, contributing beyond med chem as part of a multi-disciplinary project team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability as chemistry leader on validating or prioritizing targets with conclusive data package\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to work collaboratively with cross-functional teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to be both a strategic leader and a hands-on problem solver\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational skills, ability to multi-task in an extremely fast-paced environment with changing priorities while maintaining attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to communicate clearly and concisely with all stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Compensation\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;em\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/em\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;em\u0026gt;The anticipated base salary range for this role is $195,000 – $275,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/em\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;em\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/em\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057518003,"name":"Research","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7608846003#open-positions","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":5709440003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7608846003,"updated_at":"2026-04-14T11:30:39-04:00","requisition_id":"2641","title":"Director or Senior Director of Biostatistics","company_name":"Kymera Therapeutics","first_published":"2026-01-28T12:44:08-05:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;As the Lead Statistician, you will spearhead the statistical efforts of one or more clinical programs, playing a key role in the clinical development plan, regulatory submissions, and overall data strategy. This role requires strategic involvement in program teams, authorship of statistical sections in study documents, and direct oversight of outsourced statistical functions.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Act as the lead statistician of a clinical program, leading statistical efforts and representing biometrics functions on program teams. Make strategic contributions to the clinical development plan.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the biostatistical lead for regulatory submissions and inspections, ensuring compliance with global regulatory standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the development of clinical protocols by authoring the statistical methods section and reviewing other sections for statistical accuracy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and review statistical analysis plans for individual studies and integrated summaries of safety/efficacy (ISS/ISE). Create and edit statistical outputs shells.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide statistical input during CRF design to ensure alignment with study objectives and analyze requirements. Oversee and quality control results from statistical programmers or CROs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to clinical study reports by authoring statistical sections and interpreting study results. Support the preparation of scientific publications and presentations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage relationships with CROs to ensure high-quality statistical outputs and compliance with study requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;May manage direct reports, as needed, providing guidance and professional development.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree in Statistics or related field with minimum 6 years of clinical trial experience in a biotechnology or pharma company.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive knowledge of statistical methods for clinical trials and deep familiarity with FDA, EMA, and ICH guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise in SAS required; R or Python is advantageous. Experience with trial design software such as EAST or nQuery.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills necessary for effective collaboration with cross-functional teams. Ability to communicate statistics to non-statisticians effectively; influence and ensure adoption of robust statistical methods.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional ability to manage multiple priorities in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A strong passion for innovation in Biostatistics and continuous improvement in processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical and problem-solving abilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Positive attitude and a collaborative spirit.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $195,000 – $275,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057515003,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7734895003#open-positions","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":5766295003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7734895003,"updated_at":"2026-05-15T13:36:31-04:00","requisition_id":"2692","title":"Director, Study Start-Up","company_name":"Kymera Therapeutics","first_published":"2026-05-14T16:25:56-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll contribute:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic and operational leadership for end‑to‑end study start‑up activities across assigned clinical programs, ensuring timely, compliant, and high‑quality site activation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accountable for development, execution, and ongoing optimization of study‑specific start‑up strategies, including country selection, regulatory and ethics submissions, site feasibility and selection, contract and budget execution, and site activation readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and maintain clear start‑up timelines, metrics, and dashboards; proactively identify risks to activation timelines and drive mitigation plans to achieve first‑patient‑in (FPI) and enrollment targets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide oversight of country‑ and site‑level regulatory and ethics submissions (e.g., IRB/EC/HA), ensuring consistency with global strategy and local regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure quality, completeness, and inspection readiness of start‑up documentation, including Trial Master File (TMF) content and country‑level start‑up records, in accordance with GCP and internal SOPs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Clinical Research Organization(s) to oversee site contract and budget negotiations, ensuring alignment with approved study budgets and timely execution to support activation timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary escalation point for complex start‑up challenges, including site readiness or performance risks, regulatory delays or vendor issues; communicate status and resolution plans to senior leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to portfolio‑level planning by providing start‑up insights and recommendations to inform study design, country strategy, resourcing, and feasibility assumptions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain study start‑up processes, systems, and tools to reduce cycle times, improve quality, and enhance predictability of start‑up delivery.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure start‑up activities are conducted in compliance with global regulations, internal policies, and company quality standards, maintaining a strong focus on patient safety and data integrity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support organizational readiness for audits and inspections related to study start‑up activities, partnering with Quality Assurance as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;10+ years of experience in the biotech/pharmaceutical industry with direct experience in project management within Clinical Operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record in process improvement, clinical trial execution, and operational strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with planning, management, and oversight of activities and deliverables within Clinical Operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of clinical trial management, ICH-GCP, and regulatory compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of managing multiple projects and/or programs concurrently\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent analytical, problem-solving, and organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication and interpersonal skills with the ability to influence cross-functional stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead change and foster a culture of continuous improvement.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $195,000 – $275,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057515003,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7733671003#open-positions","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":5765739003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7733671003,"updated_at":"2026-05-14T11:47:56-04:00","requisition_id":"2688","title":"Director, Trial Master File","company_name":"Kymera Therapeutics","first_published":"2026-05-13T14:11:18-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead end-to-end implementation and configuration of the Trial Master File (TMF/eTMF) platform, including system setup, role-based access, workflows, and integration with clinical systems to ensure compliance with regulatory and inspection-readiness standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, standardize, and implement TMF business processes, SOPs, governance models, and operational workflows across clinical programs, partnering with Clinical Operations, Quality, Regulatory, and IT teams to drive consistent adoption, process efficiency, and scalable execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic and operational leadership for the end‑to‑end management of the Trial Master File (TMF) across all clinical studies, ensuring inspection readiness throughout the trial lifecycle.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the TMF subject matter expert for the organization, providing guidance to Clinical Operations, Regulatory, Quality, and cross‑functional study teams on essential document requirements and best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead oversight of eTMF systems and service providers, ensuring vendor performance, compliance with contractual obligations, and alignment with sponsor expectations for TMF management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and monitor TMF performance metrics and dashboards (e.g., completeness, timeliness, quality trends), proactively identifying risks and driving corrective actions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with Clinical Operations and study teams to ensure TMF activities are integrated into study planning and execution, from study start‑up through close‑out and inspection readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure TMF readiness to support audits, inspections, and regulatory submissions, acting as a central point of contact during TMF‑related inspection activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and execute TMF QC and periodic review activities, including oversight of completeness checks, quality issues, root‑cause analysis, and CAPA development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and drive TMF training and enablement for internal staff and vendors, ensuring consistent understanding of filing responsibilities and expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain alignment between TMF practices and clinical trial oversight, vendor oversight, and protocol deviation management, ensuring documentation supports sponsor oversight obligations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead or contribute to continuous improvement initiatives to enhance TMF quality, efficiency, and inspection readiness, including process simplification and system optimization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure timely and compliant TMF close‑out, transfer, and archival, including oversight of final reconciliation activities and long‑term record retention requirements.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;10+ years of experience in the biotech/pharmaceutical industry with direct experience in TMF management and eTMF system implementation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record in process improvement, clinical trial execution/sponsor oversight, and TMF/eTMF strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with planning, management, and oversight of activities and deliverables within Clinical Operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of clinical trial management, ICH-GCP, and regulatory compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of managing multiple projects and/or programs concurrently\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent analytical, problem-solving, and organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication and interpersonal skills with the ability to influence cross-functional stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead change and foster a culture of continuous improvement.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $195,000 – $275,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057515003,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7761760003#open-positions","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":5776318003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7761760003,"updated_at":"2026-06-03T13:33:33-04:00","requisition_id":"2698B","title":"Endpoint Systems Engineer ","company_name":"Kymera Therapeutics","first_published":"2026-06-02T15:49:23-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera Therapeutics is seeking a highly capable Desktop Engineer to serve as the L3 escalation point for endpoint and user support within our hybrid Microsoft environment. This role is central to maintaining a secure, reliable, and well-managed computing experience for employees across the organization. The engineer will handle advanced troubleshooting, modern device management with Intune, identity and authentication support, and deep Windows client diagnostics.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate brings a cloud-first mindset, with the judgment and experience to operate effectively in an environment where cloud and on-premises systems still coexist. They should understand the realities and constraints of a hybrid infrastructure while actively helping the organization move toward more modern, cloud-aligned practices. This role requires strong technical instincts, the ability to collaborate across Infrastructure, Cybersecurity, and Applications teams, and a commitment to improving the stability, security, and effectiveness of the end-user computing environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Endpoint Management \u0026amp;amp; Intune Support\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Package, deploy, and maintain Win32 applications through Microsoft Intune\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and update remediation scripts, configuration profiles, and compliance policies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Troubleshoot Autopilot enrollments, ESP issues, and device identity inconsistencies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure consistent device hygiene, lifecycle management, and operational readiness\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Identity \u0026amp;amp; Access Management\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Troubleshoot hybrid identity issues involving Entra ID, Azure AD Connect, and device join states\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support user and device identity lifecycle processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Resolve authentication failures, directory sync issues, and group-based access concerns\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to identity-related troubleshooting improvements and best practices\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Microsoft 365 Support \u0026amp;amp; Escalation\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide advanced troubleshooting for Exchange Online, Teams, SharePoint, and OneDrive\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Diagnose and resolve mail flow problems, permission conflicts, and policy inconsistencies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support configuration and lifecycle management of M365 Groups\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with cross-service issues affecting collaboration and user productivity\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Windows Client Engineering\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Diagnose OS, driver, performance, profile, and Windows Update issues using advanced tools\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze event logs and system telemetry to determine root causes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify recurring endpoint issues and recommend corrective actions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support imaging and Autopilot health by addressing underlying system issues\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Scripting \u0026amp;amp; Automation\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain PowerShell scripts for support, remediation, and automation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Use JSON and basic Graph API calls when necessary\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify opportunities to reduce manual work and improve consistency\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Security \u0026amp;amp; Compliance Support\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Apply endpoint hardening practices and configuration standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform initial triage of endpoint security alerts before escalation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with the Cybersecurity team on incident workflows and risk mitigation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain device and user compliance with organizational policies\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Networking \u0026amp;amp; Connectivity Support\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Troubleshoot DNS, VPN clients, Wi-Fi issues, and routing-related symptoms\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Determine whether issues originate from the endpoint or the broader network\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist users with connectivity problems affecting productivity\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hardware Diagnostics \u0026amp;amp; Warranty Coordination\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Use OEM diagnostic tools to identify potential hardware faults\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Distinguish hardware failures from software or configuration issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate RMAs, warranty service requests, and device replacements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Validate device health and readiness following repair or replacement\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Cross-Team Collaboration \u0026amp;amp; Documentation\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Act as an escalation point for L1 and L2 support teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Document troubleshooting procedures, runbooks, and best practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Infrastructure, Cybersecurity, and Applications teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to continuous improvement of endpoint-related processes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;5+ years supporting Windows endpoints in an enterprise environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Microsoft Intune app deployment, policy management, and device troubleshooting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong troubleshooting skills across OS, identity, and Microsoft 365 services\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;PowerShell scripting skills for automation and remediation workflows\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of hybrid Entra ID / Azure AD identity concepts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience diagnosing hardware issues and coordinating warranty repairs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with DNS, VPN, and Wi-Fi troubleshooting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with Defender for Endpoint\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Background in hybrid AD DS + Entra ID environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to regulated industry environments (biotech, pharma, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting modern endpoint and collaboration ecosystems\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Personal Attributes\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Analytical, detail-oriented, and methodical approach to problem-solving\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong ownership mentality and follow-through on escalated issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable collaborating across technical and non-technical teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Committed to delivering a high-quality end-user computing experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $115,000 – $200,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4003322003,"name":"G\u0026A","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7715350003#open-positions","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":5756414003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7715350003,"updated_at":"2026-04-27T14:59:29-04:00","requisition_id":"2673B","title":"Executive Director, Talent Acquisition","company_name":"Kymera Therapeutics","first_published":"2026-04-27T14:59:29-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;The Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is not a seat-warming role. The Executive Director, Talent Acquisition is a mission-critical hire - the person who will build and own Kymera\u0026#39;s people engine through its most consequential growth phase yet.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You\u0026#39;ll work directly with our SVP, People \u0026amp;amp; Culture to architect workforce strategy for a company actively crossing the chasm from clinical to commercial readiness. You\u0026#39;ll own the full talent acquisition function - strategy and execution - leading a high-performing team that is already delivering results. Your mandate: make it more proactive, more strategic, and more tightly connected to where the business is going.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The TA function has a very strong foundation, and your role will be to enable this team to continue to build a high- performing company with top talent. \u0026amp;nbsp;Assess where we can create efficiencies, build value-add initiatives to maximize impact and create strategies that align with our long term build.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;What You\u0026#39;ll Own:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Workforce Planning \u0026amp;amp; Strategic Leadership\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Take clear, firm ownership of workforce planning - bringing rigor and proactivity to when, how, and who Kymera hires to deliver on its business objectives. Partner closely with People Partners to ensure alignment, while making sure the planning intelligence and hiring strategy is driven by Talent Acquisition.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own and lead the annual and rolling workforce planning process in close partnership with the SVP of People \u0026amp;amp; Culture and senior business leaders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create proactive pipelining strategies for Kymera\u0026#39;s most critical and hard-to-fill roles, including Medical Directors, late-stage clinical profiles, and senior leadership succession, well before vacancies become urgent\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build forward-looking commercial hiring playbooks to ensure the team is positioned to move fast when commercialization demands it\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop trust-based partnerships across all functions and levels; engage directly with leaders to anticipate talent needs rather than react to them\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Team Leadership \u0026amp;amp; Execution\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Lead a talented TA team with the leadership presence that connects the team\u0026#39;s daily work to Kymera\u0026#39;s broader ambitions. Stay close to the work yourself: this role owns requisitions and maintains first-hand visibility into candidate quality and experience.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage, develop, and grow a strong, flexible TA team that scales to meet evolving hiring needs and organizational design requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create the leadership layer that bridges the TA function and executive leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evolve interview and assessment methodologies to support faster, more data-driven, and more equitable talent decisions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive an exceptional candidate experience as a genuine extension of Kymera\u0026#39;s culture, embodying our values of Pioneer, Collaborate \u0026amp;amp; Belong\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Analytics, Reporting \u0026amp;amp; Systems\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Build the intelligence layer that makes TA a strategic asset to the business, not just a function that fills roles.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Establish an executive-ready analytics and reporting cadence: pipeline health, time-to-fill, capacity forecasts, offer acceptance, and demographic data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Optimize talent systems including ATS and workflow automation to enhance candidate management and process efficiency\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bring genuine curiosity to AI and automation tools; evaluate and pilot solutions that make the team meaningfully more effective\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Employer Brand \u0026amp;amp; Early-Talent Community\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with Communications and People + Culture on employer branding and external communications, ensuring Kymera\u0026#39;s story reaches the right talent at the right moments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Launch co-op, internship, and student community programs in partnership with business leaders, building early-talent pipelines that match Kymera’s stage and trajectory\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;10+ years in talent acquisition, with 3+ years leading a TA function end-to-end\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Full-cycle recruiting experience in biotech or pharma, genuine passion for work and a high bar for talent\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track record of proactively owning workforce planning, not just responding to requisitions, and translating business goals into talent strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience building pipelines for senior clinical, scientific, and leadership profiles (MDs, late-stage experts, succession planning)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience building fit-for-purpose analytics, reporting cadences, and systems that drive better hiring decisions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong executive communicator who can influence without authority and operate credibly with C-suite stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Resilient self-starter who thrives in fast-paced, dynamic environments and looks at process and operations with a “right-sized” lens\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Genuinely curious about AI and automation and what it can do for TA; eager to explore and experiment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $245,000 – $335,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4003322003,"name":"G\u0026A","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7586350003#open-positions","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":5699828003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7586350003,"updated_at":"2026-05-13T09:57:44-04:00","requisition_id":"2620","title":"Principal Scientist/Associate Director, Process Chemistry","company_name":"Kymera Therapeutics","first_published":"2026-04-07T15:55:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;As an Associate Director of Drug Substance Development, you will serve as the accountable Drug Substance lead for one or more development programs, owning DS strategy, execution, and delivery from late discovery through clinical development.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Use scientific, data-drive, and risk-based approaches to clinical and commercial route and process innovation and development, guided by safety and green chemistry principles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide technical leadership and decision‑making oversight for outsourced Drug Substance development activities at CROs and CDMOs, ensuring quality, timelines, and scientific rigor.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the Drug Substance technology lead for internal and external knowledge transfers, including authoring transfer strategies, defining success criteria, and supporting manufacturing execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Drug Product and Analytical colleagues to ensure the Drug Substance physical attributes are understood, controlled, and are appropriate for Drug Product manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure stage appropriate data is generated and documented; serve as contributing author and technical reviewer of Drug Substance sections of regulatory filings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate effectively with internal and external stakeholders to deliver on program objectives.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ph.D. in Chemistry or Chemical Engineering with at least 7 years’ or B.S./ M.S. in Chemistry or Chemical Engineering with at least 12 years’ experience in Drug Substance Development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bringing small molecule assets from late discovery through mid-phase clinical trials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serving as the Drug Substance lead on fully integrated Chemistry, Manufacturing, and Control (CMC) teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Directing CRO and CDMO partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Writing and reviewing Drug Substance related technical documents.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of small molecule drug development; understand how CMC disciplines integrate and partner with associated functional areas such as Quality, Non-clinical Safety, Clinical, Regulatory, and Intellectual Property Protection.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth familiarity with phase based GMPs and manufacturing compliance requirements, regulatory guidelines and expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness and ability to work hands-on and with a sense of urgency in a fast-paced, agile environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to make sound, risk‑based scientific and business decisions in ambiguous, fast‑paced development environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to conduct, manage, and communicate risk assessments.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferable Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ability to develop data driven crystallization processes based on an understanding and application of fundamental principles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using statistical and modelling software applicable to Drug Substance Development and Manufacturing to support process understanding and decision making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and execution of process characterization with cross-functional colleagues, utilizing Quality by Design principles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable stepping into hands‑on problem solving when needed to unblock programs, while maintaining focus on strategic and technical leadership.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $160,000 – $240,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057516003,"name":"Technical Operations \u0026 Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7702031003#open-positions","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":5751187003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7702031003,"updated_at":"2026-05-18T11:39:38-04:00","requisition_id":"2671B","title":"Scientist II or Senior Scientist, Discovery Proteomics","company_name":"Kymera Therapeutics","first_published":"2026-04-15T13:00:05-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Working closely with program teams towards addressing key biology and chemistry questions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and optimize sample preparation and mass spectrometry methods for deep quantitative analysis of cell and tissue total proteomes as well as post-translational modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform maintenance, quality control and troubleshooting of instruments, including HPLCs and mass spectrometers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish robust nLC-MS-based data acquisition and analysis workflows\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide documentation, analysis, interpretation and presentation of experimental data in a clear and concise manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present scientific results and strategic recommendations to internal project teams, senior leadership, and external collaborators in a clear, concise, and influential manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Stay up to date on proteomics methods and technologies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively recognize and solve technical and scientific issues to ensure high quality proteomics data is generated for the progression of drug discovery projects.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD in Biochemistry, Biology, Chemical Biology, or a related discipline, with 3+ years of quantitative mass spectrometry-based proteomics experience, or 7+ years of industry experience in proteomics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive hands-on experience in proteomics is required including:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to independently troubleshoot, analyze, and interpret proteomics data with attention to detail, to recommend and execute next steps.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High level of proficiency in a variety of quantitative proteomics techniques including DIA, label-free quantification and peptide fragmentation methods.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintaining and troubleshooting HPLCs and mass spectrometers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing methods and performing nano LC-MS/MS experiments using Orbitrap Astral or Orbitrap Exploris 480 mass spectrometers.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;li\u0026gt;Experience in computational analysis and downstream statistical analysis software packages, such as DIANN, Perseus, R or Python, to address key program questions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in an agile, fast-paced, team-oriented environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead from the lab for activities include hit validation, lead optimization, target validation, and small molecule mechanism of action studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with PTM analysis (phosphorylation and ubiquitination), protein interaction analysis, and targeted proteomics are a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in low abundance protein isolation from complex biological samples including cells, tissue and biofluids and affinity enrichment to selectively enrich sub-proteomes and experience with automation and liquid handling systems are a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in mapping protein-protein interactions by mass spectrometry with pulldown approaches, proximity labeling and XL-MS are a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tissue culture experience with suspension and adherent cell lines is a plus\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $90,000 – $200,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057518003,"name":"Research","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7725126003#open-positions","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":5760614003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7725126003,"updated_at":"2026-05-07T14:30:10-04:00","requisition_id":"2686","title":"Senior Director, Clinical Operations ","company_name":"Kymera Therapeutics","first_published":"2026-05-05T15:21:31-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt;\u0026amp;nbsp;or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Senior Director, Clinical Operations is a leadership role responsible for overseeing and managing all aspects of clinical operations for the Phase 3 program of a high priority immunology program, KT-621.\u0026amp;nbsp; This individual will be accountable for driving the cross-functional strategy and rigorous operational execution through regulatory approval.\u0026amp;nbsp; This person possesses clinical operations expertise with a track record of success, working with peers and stakeholders. The Senior Director will be a leader in the organization who knows how to hire and manage a team internally, at our clinical sites, and with our vendors.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee the strategic planning, implementation and execution of late stage clinical trials across a key immunology program in accordance with project timelines, budget, and quality standards (including ICH GCP and local regulations)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and manage comprehensive program project plans, including but not limited to, study protocols, clinical trial budgets, timelines, enrollment and risk mitigation strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate cross functionally with internal teams, including Clinical Development, Regulatory Affairs, Biostatistics and Program Leadership to ensure alignment on clinical trial objectives and milestones\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide operational expertise and strategic input into the development of Clinical Development Plans (CDP), supporting the overall clinical strategy for the program\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accountable for robust operational strategies for all studies in the Phase 3 program, ensuring consistency as needed, including country and site mix, PR\u0026amp;amp;R and Site Engagement strategies, vendor strategy, risk based and site monitoring strategies, etc\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the point of contact for CROs and vendors, overseeing their performance and ensuring adherence to contractual agreements, timelines and quality standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with regulatory requirements, ICH-GCP requirements, and company SOPs throughout all stages of clinical trial conduct\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accountable for inspection readiness and provides appropriate guidance to Clinical Study Leads in support of inspection activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the preparation and review of clinical study documents including the Investigator Brochure, Investigational New Drug Applications (IND), study protocols, clinical study reports, applicable sections of New Drug Applications (NDA) and or Marketing Authorization Application (MAA), updates to the IND, NDA and other safety reports\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hire, train and develop the Clinical Operations KT-621Phase 3 team, fostering a culture of collaboration, accountability, continues improvement, and operational excellence\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BA/BS, preferably in a health-related field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;12+ years of experience in clinical operations within the pharmaceutical or biotechnology industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience building and leading a high-performing clinical operations team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise in global regulatory and compliance requirements for clinical research, including but not limited to, US CRF, EU CTD and ICH GCP\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple competing priorities and adapt to changes in a high-pressure environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication, interpersonal, and problem solving skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be comfortable working in a fast-paced environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $235,000 - $330,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057515003,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7691143003#open-positions","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":5746896003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7691143003,"updated_at":"2026-06-02T16:50:03-04:00","requisition_id":"2662","title":"Senior Manager, Clinical Scientist, Respiratory","company_name":"Kymera Therapeutics","first_published":"2026-04-06T13:55:09-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the execution of clinical trial protocols in Respiratory, working closely with the Clinical Science Study Lead to support high-quality and scientifically rigorous study conduct.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support day-to-day study activities, in collaboration with Clinical Operations, ensuring alignment with scientific, organizational, and regulatory standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct ongoing clinical data review and cleaning of clinical trial data to ensure data quality, integrity, and patient safety.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform medical data monitoring, including review of safety data, listings, and outputs, and partner with Data Management and Medical Development to support escalation, query generation and resolution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the identification, analysis, and interpretation of clinical data trends, communicating findings and escalating to the Clinical Science Study Lead as appropriate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the development and review of study-related documents (e.g., protocols, amendments, clinical study reports).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support interactions with investigators, CROs, and vendors during study conduct.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate within a matrix environment, collaborating with medical directors, regulatory affairs, translational medicine, clinical operations, data management, biostatistics, and other departments to drive clinical development programs forward.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s or advanced degree (MSc, PharmD, MD, PhD) in Life Sciences or related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years in pharmaceutical clinical drug development, with experience in global clinical trials and program execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in immunological diseases (e.g. asthma), with an understanding of disease biology and treatment landscapes is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth understanding of clinical development processes, regulatory requirements, and guidelines (FDA, EMEA, ICH, GCP).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong critical-thinking, problem-solving abilities and excellent medical writing skills.\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $145,000 – $215,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057515003,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7586370003#open-positions","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":5699841003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7586370003,"updated_at":"2026-04-17T12:27:05-04:00","requisition_id":"2625","title":"Senior Manager or Associate Director, Strategic Sourcing","company_name":"Kymera Therapeutics","first_published":"2026-04-15T17:32:47-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with cross-functional stakeholders in Research and Development to support sourcing strategies that align with business needs and financial and operational objectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Kymera’s functional relationship managers, Legal, and Finance to support the establishment and management of master service agreements (MSAs) and subsequent statements of work (SOWs).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain strong relationships with key vendors to support effective negotiations and positive business outcomes for Kymera. \u0026amp;nbsp;Lead Supplier Relationship Management (SRM) efforts and establish contractual foundations with preferred terms.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead negotiations of business and commercial terms with contract research organizations (CROs), contract manufacturing organizations (CMOs) and other strategic vendors, in alignment with internal stakeholder needs and company objectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and implement cost savings opportunities.\u0026amp;nbsp; Deliver tangible business impact including hard savings and cost avoidance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the development, implementation, and continuous improvement of strategic sourcing processes across the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and own request for proposal (RFP) processes, bid evaluations, and vendor selection activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct vendor diligence and support the selection of primary and secondary suppliers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help establish preferred commercial terms, discounts, and sourcing strategies across key categories and vendor networks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track sourcing activities, contract status, and vendor performance metrics to help inform decision-making and ensure operational effectiveness.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;6+ years of experience in sourcing, procurement, supplier management, outsourcing, or strategic negotiations within the biotech or pharmaceutical industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting sourcing initiatives across multiple R\u0026amp;amp;D functions, including areas such as Clinical, Translational Medicine, Research, and/or CMC.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to partner effectively with internal stakeholders and deliver high-quality customer service in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting or leading contract negotiations, including commercial terms, with CROs, CMOs and other external service providers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical and problem-solving skills, with the ability to synthesize complex information and communicate clearly to a range of stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly organized, with strong project management skills and the ability to manage multiple priorities simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective influencing skills and the ability to work cross-functionally to drive alignment and outcomes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Agile learner with the ability to quickly adapt to new tools, systems, and business needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills with the ability to build and maintain productive relationships with external vendors, partners, and internal collaborators.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $145,000 – $240,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4003322003,"name":"G\u0026A","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7748991003#open-positions","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":5770861003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7748991003,"updated_at":"2026-05-26T18:19:55-04:00","requisition_id":"25X60-2","title":"Senior Scientist or Principal Scientist, Targeted Proteomics","company_name":"Kymera Therapeutics","first_published":"2026-05-26T18:19:55-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Scientific Leadership and Experimental Strategy\u0026lt;/strong\u0026gt;:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with cross-functional project teams to define key scientific questions that can be addressed by targeted proteomics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with stakeholders to prioritize studies based on urgency and program impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translate key program questions into targeted proteomics experiments, execute studies analyze and interpret data, and communicate the findings to cross-function teams to enable program\u0026lt;em\u0026gt; decision-making.\u0026lt;/em\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Targeted Proteomics and Assay Development\u0026lt;/strong\u0026gt;:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Drive TPD research programs through development and application of targeted protein mass spectrometry (MS) assays using state-of-the-art LC-MS systems—including nano-LC and Orbitrap platforms.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate pharmacodynamic (PD) profile across a wide variety of biological matrices (e.g. cells, tissues, biofluids) from both human and preclinical species.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, optimize, qualify and transfer targeted proteomics assays to support preclinical and clinical studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Innovate and implement new targeted proteomics analysis workflows, including automated enrichment strategies, to enable sensitive, precise, and scalable protein quantification.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;External Collaboration and Communication\u0026lt;/strong\u0026gt;:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee proteomics activities at CRO partners, including assay transfer, qualification, execution, and data quality oversight.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present scientific findings and strategic recommendations to project teams, senior leadership, and external collaborators in a clear, concise, and impactful manner.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD in Biochemistry, Biology, Chemistry, or Chemical Biology with a minimum of 2 years of experience in targeted, mass spectrometry–based proteomics in an industry or startup biotech setting; \u0026lt;strong\u0026gt;or\u0026lt;/strong\u0026gt; BS/MS with 8+ years of relevant experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Domain expertise in targeted proteomics, including: \u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability in translating key biological and pharmacodynamic questions into targeted proteomics strategies that inform discovery, translational, and clinical-stage decision making within fast-paced drug discovery environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Development and deployment of highly multiplexed and sensitive PRM or MRM stable isotope–labeled peptide assays using DDA and DIA data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Development of immunoaffinity enrichment methods to enhance MS assay sensitivity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of techniques for optimizing protein recovery from complex biological matrices (cells, tissues, biofluids) derived from human and preclinical species.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operation, maintenance, and troubleshooting of nanoLC and Orbitrap MS instrumentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Quantitative analysis and report generation using Skyline and related quantitative proteomics data analysis tools.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Domain leadership with cross-functional drug discovery\u0026lt;/strong\u0026gt;:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Highly organized, solutions-oriented scientist with the ability to manage multiple priorities simultaneously while driving innovation in targeted proteomics workflows and enabling program advancement through high-impact experimental data.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Proven success collaborating effectively across multidisciplinary project teams as the proteomics subject matter expert, presenting data-driven recommendations to scientific leadership and cross-functional stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills, with the ability to convey complex scientific concepts to both technical and non-technical audiences.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience preparing reports and supporting documentation for regulatory submissions, with understanding of regulatory requirements and compliance expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing external CRO partnerships, including assay transfer, study oversight, and qualification activities ensuring delivery of high-quality pharmacodynamic data that align with project timelines.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $115,000 – $215,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057518003,"name":"Research","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7748334003#open-positions","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":5770559003,"location":{"name":"Watertown, MA"},"metadata":null,"id":7748334003,"updated_at":"2026-05-26T10:51:50-04:00","requisition_id":"2697","title":"Vice President, Pharmaceutical Development ","company_name":"Kymera Therapeutics","first_published":"2026-05-26T10:51:50-04:00","language":"en","application_deadline":null,"content":"\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Who we are:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit \u0026lt;a href=\u0026quot;https://www.kymeratx.com\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;www.kymeratx.com\u0026lt;/a\u0026gt; or follow us on \u0026lt;a href=\u0026quot;https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;X (formerly Twitter)\u0026lt;/a\u0026gt; or \u0026lt;a href=\u0026quot;http://www.linkedin.com/company/kymeratherapeutics\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;LinkedIn\u0026lt;/a\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How we work:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;PIONEER\u0026lt;/strong\u0026gt;: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;COLLABORATE\u0026lt;/strong\u0026gt;: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;BELONG\u0026lt;/strong\u0026gt;: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;How you’ll make an impact:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Define and lead the company’s pharmaceutical development strategy across the portfolio, ensuring alignment with corporate priorities and development timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic leadership for preformulation, biopharmaceutics, and formulation development activities supporting discovery, preclinical, and clinical-stage programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Champion innovation in formulation sciences and enabling technologies to address complex drug delivery and bioavailability challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive development and implementation of phase-appropriate drug product development and manufacturing strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead a high-performing Pharmaceutical Development team, in internal activities and management of an external network of CROs, CDMOs, and strategic partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish scalable processes, operational frameworks, and best practices to support portfolio growth\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic oversight of outsourced development and manufacturing activities, ensuring quality, timelines, and technical objectives are achieved\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead CMC-related regulatory strategy for drug product development activities, regulatory submissions and health authority interactions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with applicable GMP and regulatory requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Pharmaceutical Development in due diligence activities, external collaborations, and interactions with other functions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to risk assessment, resource prioritization, and investment decisions as a member of the Technical Operations leadership team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster strong cross-functional partnerships across Research, Clinical, Regulatory, Quality, Supply Chain, and Program Management to enable efficient advancement of pipeline programs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Skills and experience you’ll bring:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ph.D. in Pharmaceutics, Pharmaceutical Sciences, Chemical Engineering, or related discipline with 18+ years of relevant pharmaceutical industry experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success leading pharmaceutical development strategy from discovery through clinical development, with experience supporting commercialization readiness\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of preformulation, biopharmaceutics, formulation development, and oral solid dose drug product manufacturing for small molecules\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep expertise in formulation approaches for poorly soluble compounds, including application of enabling technologies to improve bioavailability and product performance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of advancing programs through IND and clinical development milestones and contributing to successful regulatory submissions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of GMP requirements, regulatory expectations, and evolving industry trends\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience building and managing high-performing teams and external partnerships\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to effectively engage technical teams, executive leadership, external partners, and regulatory agencies\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp; \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;em\u0026gt;Equal Employment Opportunity\u0026lt;/em\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.\u0026amp;nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span class=\u0026quot;ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak\u0026quot;\u0026gt;Compensation\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The anticipated base salary range for this role is $315,000 – $395,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4057516003,"name":"Technical Operations \u0026 Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4010236003,"name":"Watertown, MA","location":"Watertown, Massachusetts, United States","child_ids":[],"parent_id":null}]}],"meta":{"total":20}}