{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5850028004","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":5070523004,"location":{"name":"Boston, Massachusetts"},"metadata":null,"id":5850028004,"updated_at":"2026-04-10T12:50:07-04:00","requisition_id":"418","title":"Associate Director, Analytical Development","company_name":"Olema Oncology","first_published":"2026-04-06T16:57:43-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026amp;nbsp;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;Associate Director, Analytical Development\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the Associate Director of Analytical Development reporting to the Senior Director of Analytical Chemistry you will be responsible for driving progress of both early and late-stage molecules by delivering phase - appropriate analytical methods, validation and tech transfers. You will partner with cross-functionally supporting process development, formulations, CMC, and quality activities. In addition, you will bring demonstrated team playing and collaboration skills and experience operating effectively in a fast-paced, growth-stage biotech environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role can be based out of our San Francisco, CA or Boston, MA office and will \u0026lt;strong\u0026gt;require\u0026amp;nbsp;10-15%\u0026amp;nbsp;travel\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Your work will\u0026amp;nbsp;\u0026lt;em\u0026gt;primarily\u0026lt;/em\u0026gt;\u0026amp;nbsp;encompass:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Supporting analytical method development, qualification, and validation for starting materials, in-process control, process intermediates, drug\u0026amp;nbsp;substances\u0026amp;nbsp;and drug products\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conducting analytical technical review of method validation/qualification protocols, data and reports generated at CDMOs for drug substances and drug products\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reviewing and approving analytical reports or certificates of analyses from CDMOs for batch release and stability testing of drug substances and drug products\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working on stability programs, monitoring/trending stability data and establishing retest periods or shelf lives for drug substances or drug products\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Providing technical input and resolving analytical and quality control issues, deviations,\u0026amp;nbsp;OOS\u0026amp;nbsp;and OOT investigations\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supporting regulatory filings (IND, IMPD, NDA, MAA) submissions as needed \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Representing\u0026amp;nbsp;analytical Chemistry at internal and external scientific team meetings as needed\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Staying current with state-of-the art approaches and applicable global regulations and industry standards\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Ideal\u0026amp;nbsp;Candidate Profile\u0026amp;nbsp;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;A love of challenging, important work.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All\u0026amp;nbsp;employees\u0026amp;nbsp;within our company play a\u0026amp;nbsp;unique and\u0026amp;nbsp;crucial role\u0026amp;nbsp;in our success, both in\u0026amp;nbsp;accomplishing\u0026amp;nbsp;our mission and building\u0026amp;nbsp;a positive\u0026amp;nbsp;company culture. As such, we are looking for\u0026amp;nbsp;someone with\u0026amp;nbsp;the right combination of\u0026amp;nbsp;\u0026lt;em\u0026gt;knowledge\u0026lt;/em\u0026gt;,\u0026amp;nbsp;\u0026lt;em\u0026gt;experience\u0026lt;/em\u0026gt;, and\u0026amp;nbsp;\u0026lt;em\u0026gt;attributes\u0026lt;/em\u0026gt;\u0026amp;nbsp;for this role.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Knowledge\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;MS or PhD in Chemistry or\u0026amp;nbsp;equivalent\u0026amp;nbsp;scientific discipline\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise\u0026amp;nbsp;in analytical development and quality control for both drug substances\u0026amp;nbsp;(emphasis)\u0026amp;nbsp;and drug product\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of cGMP, ICH, and FDA regulations/guidance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Experience\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of\u0026amp;nbsp;7+\u0026amp;nbsp;years of relevant industry experience\u0026amp;nbsp;in\u0026amp;nbsp;small molecule drug substance\u0026amp;nbsp;and drug product\u0026amp;nbsp;analytical development and quality control, including late-stage clinical development and preparation for product registration\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in an environment that strives to ensure internal technical\u0026amp;nbsp;expertise\u0026amp;nbsp;in-house while driving CDMO capabilities to meet milestones for multiple projects\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience\u0026amp;nbsp;in partnering with cross functional teams\u0026amp;nbsp;providing analytical development leadership across programs and projects\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective written, oral communication and interpersonal skills\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attributes\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Analytical thinking with problem-solving skills and the ability to adapt to changing priorities and deadline\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated and enthusiastic; fast learner who can identify the core project challenges and expeditiously change course as\u0026amp;nbsp;required\u0026amp;nbsp;in a fast-paced\u0026amp;nbsp;organization\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Teamwork and collaboration; balances team and individual responsibilities; gives and welcomes feedback; puts success of team above own interests; supports everyone\u0026#39;s efforts to succeed; shares\u0026amp;nbsp;expertise\u0026amp;nbsp;with other\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Aspires to the highest of scientific and ethical standards\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Keen to improve processes and overcome inefficiencies\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The base pay range for this position is expected to be\u0026amp;nbsp;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;$190,000-$205,000\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; \u0026lt;/em\u0026gt;annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-MT1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4084726004,"name":"Manufacturing","child_ids":[],"parent_id":null}],"offices":[{"id":4008188004,"name":"Brannan / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4013948004,"name":"Rogers / Boston","location":"Boston, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5841398004","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":5070523004,"location":{"name":"San Francisco, California"},"metadata":null,"id":5841398004,"updated_at":"2026-04-10T12:49:53-04:00","requisition_id":"418","title":"Associate Director, Analytical Development","company_name":"Olema Oncology","first_published":"2026-03-31T13:19:26-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026amp;nbsp;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;Associate Director, Analytical Development\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the Associate Director of Analytical Development reporting to the Senior Director of Analytical Chemistry you will be responsible for driving progress of both early and late-stage molecules by delivering phase - appropriate analytical methods, validation and tech transfers. You will partner with cross-functionally supporting process development, formulations, CMC, and quality activities. In addition, you will bring demonstrated team playing and collaboration skills and experience operating effectively in a fast-paced, growth-stage biotech environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role can be based out of our San Francisco, CA or Boston, MA office and will \u0026lt;strong\u0026gt;require\u0026amp;nbsp;10-15%\u0026amp;nbsp;travel\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Your work will\u0026amp;nbsp;\u0026lt;em\u0026gt;primarily\u0026lt;/em\u0026gt;\u0026amp;nbsp;encompass:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Supporting analytical method development, qualification, and validation for starting materials, in-process control, process intermediates, drug\u0026amp;nbsp;substances\u0026amp;nbsp;and drug products\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conducting analytical technical review of method validation/qualification protocols, data and reports generated at CDMOs for drug substances and drug products\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reviewing and approving analytical reports or certificates of analyses from CDMOs for batch release and stability testing of drug substances and drug products\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working on stability programs, monitoring/trending stability data and establishing retest periods or shelf lives for drug substances or drug products\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Providing technical input and resolving analytical and quality control issues, deviations,\u0026amp;nbsp;OOS\u0026amp;nbsp;and OOT investigations\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supporting regulatory filings (IND, IMPD, NDA, MAA) submissions as needed \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Representing\u0026amp;nbsp;analytical Chemistry at internal and external scientific team meetings as needed\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Staying current with state-of-the art approaches and applicable global regulations and industry standards\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Ideal\u0026amp;nbsp;Candidate Profile\u0026amp;nbsp;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;A love of challenging, important work.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All\u0026amp;nbsp;employees\u0026amp;nbsp;within our company play a\u0026amp;nbsp;unique and\u0026amp;nbsp;crucial role\u0026amp;nbsp;in our success, both in\u0026amp;nbsp;accomplishing\u0026amp;nbsp;our mission and building\u0026amp;nbsp;a positive\u0026amp;nbsp;company culture. As such, we are looking for\u0026amp;nbsp;someone with\u0026amp;nbsp;the right combination of\u0026amp;nbsp;\u0026lt;em\u0026gt;knowledge\u0026lt;/em\u0026gt;,\u0026amp;nbsp;\u0026lt;em\u0026gt;experience\u0026lt;/em\u0026gt;, and\u0026amp;nbsp;\u0026lt;em\u0026gt;attributes\u0026lt;/em\u0026gt;\u0026amp;nbsp;for this role.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Knowledge\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;MS or PhD in Chemistry or\u0026amp;nbsp;equivalent\u0026amp;nbsp;scientific discipline\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise\u0026amp;nbsp;in analytical development and quality control for both drug substances\u0026amp;nbsp;(emphasis)\u0026amp;nbsp;and drug product\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of cGMP, ICH, and FDA regulations/guidance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Experience\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of\u0026amp;nbsp;7+\u0026amp;nbsp;years of relevant industry experience\u0026amp;nbsp;in\u0026amp;nbsp;small molecule drug substance\u0026amp;nbsp;and drug product\u0026amp;nbsp;analytical development and quality control, including late-stage clinical development and preparation for product registration\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in an environment that strives to ensure internal technical\u0026amp;nbsp;expertise\u0026amp;nbsp;in-house while driving CDMO capabilities to meet milestones for multiple projects\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience\u0026amp;nbsp;in partnering with cross functional teams\u0026amp;nbsp;providing analytical development leadership across programs and projects\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective written, oral communication and interpersonal skills\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attributes\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Analytical thinking with problem-solving skills and the ability to adapt to changing priorities and deadline\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated and enthusiastic; fast learner who can identify the core project challenges and expeditiously change course as\u0026amp;nbsp;required\u0026amp;nbsp;in a fast-paced\u0026amp;nbsp;organization\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Teamwork and collaboration; balances team and individual responsibilities; gives and welcomes feedback; puts success of team above own interests; supports everyone\u0026#39;s efforts to succeed; shares\u0026amp;nbsp;expertise\u0026amp;nbsp;with other\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Aspires to the highest of scientific and ethical standards\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Keen to improve processes and overcome inefficiencies\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The base pay range for this position is expected to be\u0026amp;nbsp;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;$190,000-$205,000\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; \u0026lt;/em\u0026gt;annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-MT1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4084726004,"name":"Manufacturing","child_ids":[],"parent_id":null}],"offices":[{"id":4008188004,"name":"Brannan / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4013948004,"name":"Rogers / Boston","location":"Boston, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5818437004","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":5059198004,"location":{"name":"Boston, Massachusetts"},"metadata":null,"id":5818437004,"updated_at":"2026-04-22T13:20:21-04:00","requisition_id":"401","title":"Associate Director, Clinical Supply Chain","company_name":"Olema Oncology","first_published":"2026-03-05T17:12:29-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role \u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp; Associate Director, Clinical Supply Chain\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the Associate Director of Clinical Supply Chain reporting to the Vice President, Clinical Supply Chain, you will plan, create, implement, build, and optimize the clinical supply chain to ensure uninterrupted and timely clinical drug supply for Olema’s clinical programs.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is available in either our San Francisco or Cambridge office and will require about 15% domestic or international travel.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Your work will\u0026amp;nbsp;\u0026lt;em\u0026gt;primarily\u0026lt;/em\u0026gt;\u0026amp;nbsp;encompass:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;End to End clinical supply chain management\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement global Clinical Supply Chain strategies\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage global inventories, shipping, and third-party manufacturers /\u0026amp;nbsp;logistics\u0026amp;nbsp;providers\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and manage Interactive Response Technologies (IRT) systems\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversight packaging, labeling, and distribution activities at multiple vendors\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate and manage clinical labels\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify\u0026amp;nbsp;supply chain risks, escalate if needed, and close out risk items\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Clinical Operations to align on assumptions and build clinical supply to meet program demand\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Clinical Supply Chain on study execution teams\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Knowledge:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree is\u0026amp;nbsp;required,\u0026amp;nbsp;Master’s\u0026amp;nbsp;degree is preferred\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Late phase clinical development and clinical supply chain management\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thorough knowledge of Good Manufacturing Practices (GMP)\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Experience:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;8+ years of biotechnology/pharmaceutical industry experience\u0026lt;em\u0026gt;\u0026amp;nbsp;\u0026lt;/em\u0026gt;in clinical supply chain management\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Inventory management and third-party\u0026amp;nbsp;logistics\u0026amp;nbsp;oversight experience\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience managing forecast demands\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience managing global, large, late-stage studies with standard of care drugs\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong global shipping and customs experience\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid experience developing clinical labels\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience developing IRT specifications\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience and troubleshooting\u0026amp;nbsp;proficiency\u0026amp;nbsp;with QMS and\u0026amp;nbsp;purchasing\u0026amp;nbsp;systems\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience in oncology trials using small molecules is preferred\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent project management skills\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Attributes:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication and skills\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analytical thinking with problem-solving skills and the ability to adapt to changing priorities and deadlines\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A commitment to excellence\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated and enthusiastic; fast learner who can identify the core project challenges and expeditiously change course as\u0026amp;nbsp;required\u0026amp;nbsp;in a fast-paced organization\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Teamwork and collaboration; balances team and individual responsibilities; gives and welcomes feedback; puts success of team above own interests; supports everyone\u0026#39;s efforts to succeed; shares\u0026amp;nbsp;expertise\u0026amp;nbsp;with others\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Entrepreneurial mindset and the ability to prioritize key work streams and requirements that will change over the near and mid-term\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A demonstrated ability to make decisions on incomplete information and in areas where a high degree of professional judgment is\u0026amp;nbsp;required\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Be a “difference maker” in terms of one’s professionalism and contributions\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Have impeccable professional ethics,\u0026amp;nbsp;integrity\u0026amp;nbsp;and judgment\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Be collegial, hard-working, confident, a self-starter and have a passion for results\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The base pay range for this position is expected to be \u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;$185,000 - $200,000\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;annually,\u0026amp;nbsp;however\u0026amp;nbsp;the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-CK1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4084726004,"name":"Manufacturing","child_ids":[],"parent_id":null}],"offices":[{"id":4008188004,"name":"Brannan / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4008187004,"name":"Owens / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4013948004,"name":"Rogers / Boston","location":"Boston, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5818438004","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":5059198004,"location":{"name":"San Francisco, California"},"metadata":null,"id":5818438004,"updated_at":"2026-04-22T13:20:22-04:00","requisition_id":"401","title":"Associate Director, Clinical Supply Chain","company_name":"Olema Oncology","first_published":"2026-03-05T17:12:30-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role \u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp; Associate Director, Clinical Supply Chain\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the Associate Director of Clinical Supply Chain reporting to the Vice President, Clinical Supply Chain, you will plan, create, implement, build, and optimize the clinical supply chain to ensure uninterrupted and timely clinical drug supply for Olema’s clinical programs.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is available in either our San Francisco or Cambridge office and will require about 15% domestic or international travel.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Your work will\u0026amp;nbsp;\u0026lt;em\u0026gt;primarily\u0026lt;/em\u0026gt;\u0026amp;nbsp;encompass:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;End to End clinical supply chain management\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement global Clinical Supply Chain strategies\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage global inventories, shipping, and third-party manufacturers /\u0026amp;nbsp;logistics\u0026amp;nbsp;providers\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and manage Interactive Response Technologies (IRT) systems\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversight packaging, labeling, and distribution activities at multiple vendors\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate and manage clinical labels\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify\u0026amp;nbsp;supply chain risks, escalate if needed, and close out risk items\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Clinical Operations to align on assumptions and build clinical supply to meet program demand\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Clinical Supply Chain on study execution teams\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Knowledge:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree is\u0026amp;nbsp;required,\u0026amp;nbsp;Master’s\u0026amp;nbsp;degree is preferred\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Late phase clinical development and clinical supply chain management\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thorough knowledge of Good Manufacturing Practices (GMP)\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Experience:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;8+ years of biotechnology/pharmaceutical industry experience\u0026lt;em\u0026gt;\u0026amp;nbsp;\u0026lt;/em\u0026gt;in clinical supply chain management\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Inventory management and third-party\u0026amp;nbsp;logistics\u0026amp;nbsp;oversight experience\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience managing forecast demands\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience managing global, large, late-stage studies with standard of care drugs\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong global shipping and customs experience\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid experience developing clinical labels\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience developing IRT specifications\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience and troubleshooting\u0026amp;nbsp;proficiency\u0026amp;nbsp;with QMS and\u0026amp;nbsp;purchasing\u0026amp;nbsp;systems\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience in oncology trials using small molecules is preferred\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent project management skills\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Attributes:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication and skills\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analytical thinking with problem-solving skills and the ability to adapt to changing priorities and deadlines\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A commitment to excellence\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated and enthusiastic; fast learner who can identify the core project challenges and expeditiously change course as\u0026amp;nbsp;required\u0026amp;nbsp;in a fast-paced organization\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Teamwork and collaboration; balances team and individual responsibilities; gives and welcomes feedback; puts success of team above own interests; supports everyone\u0026#39;s efforts to succeed; shares\u0026amp;nbsp;expertise\u0026amp;nbsp;with others\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Entrepreneurial mindset and the ability to prioritize key work streams and requirements that will change over the near and mid-term\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A demonstrated ability to make decisions on incomplete information and in areas where a high degree of professional judgment is\u0026amp;nbsp;required\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Be a “difference maker” in terms of one’s professionalism and contributions\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Have impeccable professional ethics,\u0026amp;nbsp;integrity\u0026amp;nbsp;and judgment\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Be collegial, hard-working, confident, a self-starter and have a passion for results\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The base pay range for this position is expected to be \u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;$185,000 - $200,000\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;annually,\u0026amp;nbsp;however\u0026amp;nbsp;the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-CK1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4084726004,"name":"Manufacturing","child_ids":[],"parent_id":null}],"offices":[{"id":4008188004,"name":"Brannan / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4008187004,"name":"Owens / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4013948004,"name":"Rogers / Boston","location":"Boston, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5840034004","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":5069828004,"location":{"name":"Dublin, Ireland"},"metadata":null,"id":5840034004,"updated_at":"2026-04-09T11:59:07-04:00","requisition_id":"413","title":"Director, CMC Drug Substance Manufacturing","company_name":"Olema Oncology","first_published":"2026-03-31T10:11:47-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;About the Role \u0026amp;gt;\u0026amp;gt;\u0026amp;gt; Director, CMC Drug Substance Manufacturing\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the Director, CMC Drug Substance Manufacturing reporting to the Sr Director, Drug Substance Development and Manufacturing, you will provide technical leadership and hands-on execution to support late-stage development, technology transfer to CDMOs, and commercial readiness including NDA filing for small molecule drug substances. This role is critical to ensuring successful scale-up, validation, and regulatory approval of drug substance processes. The individual will work cross-functionally and externally with CDMOs to deliver robust, compliant, and efficient manufacturing processes suitable for commercial supply.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based out of our Dublin, Ireland office and will require 10-15% travel.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Your work will\u0026amp;nbsp;\u0026lt;em\u0026gt;primarily\u0026lt;/em\u0026gt;\u0026amp;nbsp;encompass:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead technology transfer of drug substance processes (RSM/API) to CDMOs, including strategy, execution, and risk management to support late-stage development and commercial manufacturing\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide technical oversight of CDMO activities, including process validation, manufacturing campaigns, and on-site support; serve as the primary technical point of contact\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and approve key manufacturing and development documentation (batch records, protocols, reports, specifications, and deviations) to ensure compliance and data integrity\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead deviation investigations, root cause analysis, and implementation of corrective and preventive actions (CAPAs) to support reliable manufacturing performance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive process robustness, control strategy development (e.g., DOE, PAR), and PPQ readiness to enable successful validation and commercial supply\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leverage process and manufacturing data to enhance process understanding,\u0026amp;nbsp;monitor\u0026amp;nbsp;performance across sites, and\u0026amp;nbsp;identify\u0026amp;nbsp;opportunities for continuous improvement\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support commercial supply readiness, including supply continuity, cost of goods optimization, and lifecycle management activities\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and review CMC sections of IND/NDA submissions, and support regulatory interactions, responses, and inspection readiness\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify\u0026amp;nbsp;technical risks and proactively develop mitigation strategies to ensure timelines for NDA filing and commercial launch are achieved\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner cross-functionally with Quality, Regulatory, Analytical, Drug Product, and Supply Chain to ensure aligned execution and compliance with global regulatory requirements\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Ideal Candidate Profile \u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;A love of challenging, important work.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All\u0026amp;nbsp;employees\u0026amp;nbsp;within our company play a\u0026amp;nbsp;unique and\u0026amp;nbsp;crucial role\u0026amp;nbsp;in our success, both in\u0026amp;nbsp;accomplishing\u0026amp;nbsp;our mission and building\u0026amp;nbsp;a positive\u0026amp;nbsp;company culture. As such, we are looking for\u0026amp;nbsp;someone with\u0026amp;nbsp;the right combination of\u0026amp;nbsp;\u0026lt;em\u0026gt;knowledge\u0026lt;/em\u0026gt;,\u0026amp;nbsp;\u0026lt;em\u0026gt;experience\u0026lt;/em\u0026gt;, and\u0026amp;nbsp;\u0026lt;em\u0026gt;attributes\u0026lt;/em\u0026gt;\u0026amp;nbsp;for this role.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Knowledge\u0026amp;nbsp;and experience:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ph.D. in Organic Chemistry or related discipline with ~10+ years of experience (or M.S. with ~15+ years) in small molecule CMC drug substance development and manufacturing\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience leading technology transfer, scale-up, and validation of API processes to GMP manufacturing sites for late-stage and commercial programs\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong experience managing CDMOs, including vendor selection, technical oversight, and delivery of manufacturing campaigns aligned with quality, timeline, and cost objectives\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success authoring and reviewing CMC sections of INDs, IMPDs, and NDAs/MAAs, and supporting regulatory interactions and responses with health authorities\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong technical foundation in small molecule process development, manufacturing, and control strategy, including DOE, PAR, and impurity control (e.g., fate and purge)\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of cGMP requirements and global regulatory expectations (ICH guidelines), with experience supporting inspection readiness and compliant manufacturing execution\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to\u0026amp;nbsp;identify\u0026amp;nbsp;technical risks and apply risk-based decision-making to drive\u0026amp;nbsp;timely\u0026amp;nbsp;and practical solutions\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience integrating process and manufacturing data to support process understanding, trend analysis, and continuous improvement\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management and communication skills, with the ability to influence cross-functional teams and external partners in a matrixed environment\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Attributes:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Curious, scientifically rigorous, and proactive with a strong “can-do” mindset\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated and accountable, able to work independently and drive results\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective collaborator across cross-functional teams and external partners\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly analytical and detail-oriented, with a data-driven approach\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organized and execution-focused, able to manage multiple priorities and timelines\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Committed to high scientific, quality, and ethical standards while driving continuous improvement\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-MK1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4084726004,"name":"Manufacturing","child_ids":[],"parent_id":null}],"offices":[{"id":4091823004,"name":"Dublin / Ireland","location":"County Dublin, Ireland","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5742005004","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":5022200004,"location":{"name":"San Francisco, California"},"metadata":null,"id":5742005004,"updated_at":"2026-05-15T18:03:15-04:00","requisition_id":"392","title":"Director of Facilities and Laboratory Operations","company_name":"Olema Oncology","first_published":"2025-12-22T13:52:40-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role \u0026amp;gt;\u0026amp;gt;\u0026amp;gt; Director of Facilities and Laboratory Operations\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;As the Director of Facilities, Laboratory Operations reporting to the VP of IT, Real Estate, and Facilities Lab Operations, you will play a critical leadership role in shaping and scaling the environments that power Olema’s science and innovation. You will lead the strategy, operations, and long-term planning for Olema’s facilities and laboratory infrastructure across multiple sites, ensuring our spaces evolve alongside the company’s ambitious growth trajectory.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:210,\u0026amp;quot;335559739\u0026amp;quot;:210}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;In this role, you will own the full lifecycle of facilities and laboratory operations — from driving day-to-day operational excellence to leading complex, high-impact initiatives including laboratory buildouts, expansions, and office and lab relocations. You will oversee three Olema locations spanning BSL-2 laboratory environments and corporate office space, creating safe, efficient, and collaborative environments where teams can do their best work.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:210,\u0026amp;quot;335559739\u0026amp;quot;:210}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;As a trusted cross-functional partner to Research, IT, Real Estate, Finance and Executive Leadership, you will help build the operational foundation that enables Olema to scale with agility, support groundbreaking science, and foster a culture of innovation, safety, and continuous improvement.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:210,\u0026amp;quot;335559739\u0026amp;quot;:210}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based in our San Francisco office and will require\u0026amp;nbsp;15%\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;travel.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Your work will\u0026amp;nbsp;\u0026lt;em\u0026gt;primarily\u0026lt;/em\u0026gt; encompass:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Facilities, Real Estate \u0026amp;amp; Capital Execution\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and execute all\u0026amp;nbsp;facilities\u0026amp;nbsp;operations and physical infrastructure activities across Olema’s locations\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own the execution of Real Estate strategy, including site readiness, lease transitions, expansions, consolidations, and exits\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead office and laboratory\u0026amp;nbsp;moves\u0026amp;nbsp;and building relocations, with full accountability for planning, execution, risk management, and stabilization\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct laboratory and office\u0026amp;nbsp;buildouts\u0026amp;nbsp;end-to-end, from programming and design through permitting, construction, commissioning, and occupancy\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute capital projects in active lab environments while\u0026amp;nbsp;maintaining\u0026amp;nbsp;safety, compliance, and continuity of scientific operations\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and enforce facilities standards, policies, procedures, and SOPs\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own physical security programs, including access control, badging, alarms, vendor oversight, and incident response\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Control facilities\u0026amp;nbsp;operating\u0026amp;nbsp;and capital budgets, including forecasting, spend management, and cost accountability\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead emergency planning and response across all facilities\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct shipping and receiving operations, including Hazardous Materials and Dangerous Goods compliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own all workplace services across all locations, including office supplies, beverage and food programs, janitorial services, and waste management, with accountability for vendor performance, cost control, and service quality\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Laboratory Operations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support the research team with all infrastructure needs, including vendor relationships and management, service and maintenance of scientific equipment, hazardous waste management, and cell culture support\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor critical systems and provide 24-hour on-call support in case of system failure\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and\u0026amp;nbsp;maintain\u0026amp;nbsp;awareness of health and safety issues within the company, ensure compliance with company policies through\u0026amp;nbsp;appropriate training\u0026amp;nbsp;of employees, and manage safety consultants effectively.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage and Maintain\u0026amp;nbsp;Cryo\u0026amp;nbsp;storage, liquid nitrogen, compressed gas system, emergency generator system,\u0026amp;nbsp;vacuum\u0026amp;nbsp;and compressed air systems\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage critical laboratory systems, including but not limited to HVAC, monitoring, systems and equipment maintenance, to ensure uninterrupted functionality and optimal performance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee all aspects of shipping and receiving operations, including inventory management, packaging, and transportation logistics, to facilitate efficient and timely movement of goods\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and execute laboratory operations to ensure uninterrupted, compliant research support\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Environmental Health \u0026amp;amp; Safety (EHS) Ownership\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Accountable owner of Olema’s Environmental Health and Safety program\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design, implement, enforce, and continuously improve EHS policies, procedures, training, and compliance programs\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead all regulatory inspections, audits, and agency interactions\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own hazardous waste permitting, reporting, corrective actions, and compliance documentation\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Embed EHS requirements into lab design, construction, moves, and daily operations\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct EHS consultants and contractors with clear accountability for outcomes\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain, train\u0026amp;nbsp;and scale EHS programs supporting BSL-2 laboratory environments\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Ideal Candidate Profile:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;A love of challenging, important work.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees within our company play a unique and crucial role in our success, both in\u0026amp;nbsp;accomplishing\u0026amp;nbsp;our mission and building a positive company culture. As such, we are looking for someone with the right combination of\u0026amp;nbsp;\u0026lt;em\u0026gt;knowledge\u0026lt;/em\u0026gt;,\u0026amp;nbsp;\u0026lt;em\u0026gt;experience\u0026lt;/em\u0026gt;, and\u0026amp;nbsp;\u0026lt;em\u0026gt;attributes\u0026lt;/em\u0026gt;\u0026amp;nbsp;for this role.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Knowledge\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s Degree required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic\u0026amp;nbsp;Facilities Manager (SFM) and Certified Safety\u0026amp;nbsp;Professional\u0026amp;nbsp;(CSP)\u0026amp;nbsp;certifications\u0026amp;nbsp;required\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven\u0026amp;nbsp;track record\u0026amp;nbsp;of successful facilities leadership experience\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expert-level knowledge of facilities, laboratory operations, and EHS in biotech or life sciences\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management, planning, organization, and time management skills\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Experience\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of\u0026amp;nbsp;10+\u0026amp;nbsp;years of experience with a minimum\u0026amp;nbsp;of\u0026amp;nbsp;5 years of facilities management\u0026amp;nbsp;experience, including oversight of lab environments\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Created and ran an EHS program for a BSL2 Lab a must have\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ownership of lab\u0026amp;nbsp;buildouts\u0026amp;nbsp;relocations, and real estate execution\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on facilities, lab operations, and leadership experience\u0026amp;nbsp;who can move seamlessly between strategic planning and tactical execution, particularly in challenging laboratory settings that require sound judgment, calm decision-making, and rigorous operational discipline\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience working in a demanding and fast-paced lab environment where uptime, safety, compliance, and responsiveness are critical, and where competing priorities and situational ambiguity are the norm rather than the exception\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Attributes\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Highly organized with strong attention to detail, clarity, and accuracy\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solutions-oriented with a meticulous eye for detail and thrives in a fast-paced, problem-solving environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive, self-motivated, and results-oriented with a \u0026quot;bias for action\u0026quot;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative team player who thrives in a cross-functional environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible and adaptable to evolving business needs and technology trends\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written verbal and interpersonal\u0026amp;nbsp;communication skills and ability to adapt communication styles to varied internal and external partners\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The base pay range for this position is expected to be \u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;$210,000 - $220,000\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-MT1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4023658004,"name":"Business and Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4008188004,"name":"Brannan / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4008187004,"name":"Owens / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4013948004,"name":"Rogers / Boston","location":"Boston, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5848133004","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":5073235004,"location":{"name":"San Francisco, California"},"metadata":null,"id":5848133004,"updated_at":"2026-04-10T12:53:43-04:00","requisition_id":"427","title":"Lead Senior Medical Writer","company_name":"Olema Oncology","first_published":"2026-04-03T13:27:42-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role \u0026amp;gt;\u0026amp;gt;\u0026amp;gt; Lead Senior Medical Writer\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the Lead Senior Medical Writer, reporting to the Director of Medical Writing, you will lead the development, and delivery of high-quality scientific and regulatory documents supporting Olema’s oncology portfolio. This role requires strong cross-functional leadership, partnering closely with Clinical Science, Clinical Development, Regulatory Affairs, Biometrics, and other stakeholders to translate complex clinical and preclinical data into clear, accurate, and compelling content for regulatory submissions, medical communications, and scientific publications. In addition, you will drive consistency, quality, and timelines across deliverables, contributing to the overall medical writing strategy and supporting key regulatory and clinical milestones.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role\u0026amp;nbsp;is\u0026amp;nbsp;based out of our\u0026amp;nbsp;\u0026lt;strong\u0026gt;Boston, MA or San Francisco, CA\u0026lt;/strong\u0026gt;\u0026amp;nbsp;office and will require\u0026amp;nbsp;\u0026lt;strong\u0026gt;10-15%\u0026amp;nbsp;travel\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Your work will\u0026amp;nbsp;\u0026lt;em\u0026gt;primarily\u0026lt;/em\u0026gt;\u0026amp;nbsp;encompass:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Preparing and editing a wide range of scientific and medical writing deliverables, including but not limited to protocols, protocol amendments, clinical study protocols, investigator brochures, regulatory submission documents (e.g. IBs, DSURs, sections of IND/IMPD/MAAs), PowerPoint presentations related to the Medical Writing function\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborating with internal stakeholders (clinical scientists, regulatory strategy, medical monitors, biometrics, medical affairs) to understand data, interpret results, and ensure accurate message conveyance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensuring documents adhere to internal style guidelines, regulatory requirements (e.g., ICH, GPP), and appropriate therapeutic-area standards (e.g., oncology, breast cancer)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintaining version control, track author/reviewer feedback, and delivering documents according to project timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Providing  writing and/or QC editing support for associated submission documents (as applicable) to help elevate overall team deliverables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Remaining current on therapeutic area (breast cancer / endocrine-driven tumors) trends, journal publications, and regulatory guidance relevant to oncology and women’s cancers\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Ideal\u0026amp;nbsp;Candidate Profile \u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;A love of challenging, important work.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All\u0026amp;nbsp;employees\u0026amp;nbsp;within our company play a\u0026amp;nbsp;unique and\u0026amp;nbsp;crucial role\u0026amp;nbsp;in our success, both in\u0026amp;nbsp;accomplishing\u0026amp;nbsp;our mission and building\u0026amp;nbsp;a positive\u0026amp;nbsp;company culture. As such, we are looking for\u0026amp;nbsp;someone with\u0026amp;nbsp;the right combination of\u0026amp;nbsp;\u0026lt;em\u0026gt;knowledge\u0026lt;/em\u0026gt;,\u0026amp;nbsp;\u0026lt;em\u0026gt;experience\u0026lt;/em\u0026gt;, and\u0026amp;nbsp;\u0026lt;em\u0026gt;attributes\u0026lt;/em\u0026gt;\u0026amp;nbsp;for this role.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Knowledge:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in life sciences, pharmacy, or related field; advanced degree (MS/PharmD/PhD) preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated and excellent scientific writing and editing skills —\u0026amp;nbsp;the ability\u0026amp;nbsp;to translate complex\u0026amp;nbsp;scientific data into clear,\u0026amp;nbsp;concise, accurate documents for varied audiences (regulatory agencies, KOLs, internal stakeholders)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory writing standards (e.g., ICH E3/E6,\u0026amp;nbsp;GPP)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oncology preferred\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Veeva RIM experience\u0026amp;nbsp;is a plus\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Experience:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of\u0026amp;nbsp;7+\u0026amp;nbsp;years of medical or regulatory writing experience, oncology (especially breast cancer)\u0026amp;nbsp;preferred, or\u0026amp;nbsp;a closely related therapeutic area\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management skills: able to manage multiple deliverables, meet deadlines, handle feedback iterations, and coordinate with cross-functional teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently with minimal supervision, while also being a collaborative team player\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented, organized, with strong verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with standard technical and document-management tools (e.g., Microsoft Word, PowerPoint, Microsoft Excel, Smartsheet, Starting Point Templates, Veeva RIM)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience in clinical-trial documentation for oncology (eg, IBs, protocols, DSUR and CSRs) preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in hybrid/remote environments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Attributes:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Teamwork and collaboration; balances team and individual responsibilities; gives and welcomes feedback; puts success of team above own interests; supports everyone\u0026#39;s efforts to succeed; shares expertise with others\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated and enthusiastic; fast learner who can identify project challenges and expeditiously change course as required in a fast-paced organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communicator who can tailor messaging to diverse audiences\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly organized with strong attention to detail and follow-through\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability in building strong cross functional working relationships\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The base pay range for this position is expected to be\u0026amp;nbsp;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;$160,000-$175,000\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; \u0026lt;/em\u0026gt;annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-MT1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4023657004,"name":"Clinical","child_ids":[],"parent_id":null}],"offices":[{"id":4008187004,"name":"Owens / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4013948004,"name":"Rogers / Boston","location":"Boston, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5848134004","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":5073235004,"location":{"name":"Boston, Massachusetts"},"metadata":null,"id":5848134004,"updated_at":"2026-04-10T12:53:55-04:00","requisition_id":"427","title":"Lead Senior Medical Writer","company_name":"Olema Oncology","first_published":"2026-04-03T13:27:43-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role \u0026amp;gt;\u0026amp;gt;\u0026amp;gt; Lead Senior Medical Writer\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the Lead Senior Medical Writer, reporting to the Director of Medical Writing, you will lead the development, and delivery of high-quality scientific and regulatory documents supporting Olema’s oncology portfolio. This role requires strong cross-functional leadership, partnering closely with Clinical Science, Clinical Development, Regulatory Affairs, Biometrics, and other stakeholders to translate complex clinical and preclinical data into clear, accurate, and compelling content for regulatory submissions, medical communications, and scientific publications. In addition, you will drive consistency, quality, and timelines across deliverables, contributing to the overall medical writing strategy and supporting key regulatory and clinical milestones.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role\u0026amp;nbsp;is\u0026amp;nbsp;based out of our\u0026amp;nbsp;\u0026lt;strong\u0026gt;Boston, MA or San Francisco, CA\u0026lt;/strong\u0026gt;\u0026amp;nbsp;office and will require\u0026amp;nbsp;\u0026lt;strong\u0026gt;10-15%\u0026amp;nbsp;travel\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Your work will\u0026amp;nbsp;\u0026lt;em\u0026gt;primarily\u0026lt;/em\u0026gt;\u0026amp;nbsp;encompass:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Preparing and editing a wide range of scientific and medical writing deliverables, including but not limited to protocols, protocol amendments, clinical study protocols, investigator brochures, regulatory submission documents (e.g. IBs, DSURs, sections of IND/IMPD/MAAs), PowerPoint presentations related to the Medical Writing function\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborating with internal stakeholders (clinical scientists, regulatory strategy, medical monitors, biometrics, medical affairs) to understand data, interpret results, and ensure accurate message conveyance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensuring documents adhere to internal style guidelines, regulatory requirements (e.g., ICH, GPP), and appropriate therapeutic-area standards (e.g., oncology, breast cancer)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintaining version control, track author/reviewer feedback, and delivering documents according to project timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Providing  writing and/or QC editing support for associated submission documents (as applicable) to help elevate overall team deliverables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Remaining current on therapeutic area (breast cancer / endocrine-driven tumors) trends, journal publications, and regulatory guidance relevant to oncology and women’s cancers\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Ideal\u0026amp;nbsp;Candidate Profile \u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;A love of challenging, important work.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All\u0026amp;nbsp;employees\u0026amp;nbsp;within our company play a\u0026amp;nbsp;unique and\u0026amp;nbsp;crucial role\u0026amp;nbsp;in our success, both in\u0026amp;nbsp;accomplishing\u0026amp;nbsp;our mission and building\u0026amp;nbsp;a positive\u0026amp;nbsp;company culture. As such, we are looking for\u0026amp;nbsp;someone with\u0026amp;nbsp;the right combination of\u0026amp;nbsp;\u0026lt;em\u0026gt;knowledge\u0026lt;/em\u0026gt;,\u0026amp;nbsp;\u0026lt;em\u0026gt;experience\u0026lt;/em\u0026gt;, and\u0026amp;nbsp;\u0026lt;em\u0026gt;attributes\u0026lt;/em\u0026gt;\u0026amp;nbsp;for this role.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Knowledge:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in life sciences, pharmacy, or related field; advanced degree (MS/PharmD/PhD) preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated and excellent scientific writing and editing skills —\u0026amp;nbsp;the ability\u0026amp;nbsp;to translate complex\u0026amp;nbsp;scientific data into clear,\u0026amp;nbsp;concise, accurate documents for varied audiences (regulatory agencies, KOLs, internal stakeholders)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory writing standards (e.g., ICH E3/E6,\u0026amp;nbsp;GPP)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oncology preferred\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Veeva RIM experience\u0026amp;nbsp;is a plus\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Experience:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of\u0026amp;nbsp;7+\u0026amp;nbsp;years of medical or regulatory writing experience, oncology (especially breast cancer)\u0026amp;nbsp;preferred, or\u0026amp;nbsp;a closely related therapeutic area\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management skills: able to manage multiple deliverables, meet deadlines, handle feedback iterations, and coordinate with cross-functional teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently with minimal supervision, while also being a collaborative team player\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented, organized, with strong verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with standard technical and document-management tools (e.g., Microsoft Word, PowerPoint, Microsoft Excel, Smartsheet, Starting Point Templates, Veeva RIM)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience in clinical-trial documentation for oncology (eg, IBs, protocols, DSUR and CSRs) preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in hybrid/remote environments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Attributes:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Teamwork and collaboration; balances team and individual responsibilities; gives and welcomes feedback; puts success of team above own interests; supports everyone\u0026#39;s efforts to succeed; shares expertise with others\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated and enthusiastic; fast learner who can identify project challenges and expeditiously change course as required in a fast-paced organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communicator who can tailor messaging to diverse audiences\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly organized with strong attention to detail and follow-through\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability in building strong cross functional working relationships\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The base pay range for this position is expected to be\u0026amp;nbsp;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;$160,000-$175,000\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; \u0026lt;/em\u0026gt;annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-MT1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4023657004,"name":"Clinical","child_ids":[],"parent_id":null}],"offices":[{"id":4008187004,"name":"Owens / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4013948004,"name":"Rogers / Boston","location":"Boston, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5842651004","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":5071061004,"location":{"name":"San Francisco, California"},"metadata":null,"id":5842651004,"updated_at":"2026-05-15T18:47:02-04:00","requisition_id":"421","title":"Senior Clinical Trial Associate ","company_name":"Olema Oncology","first_published":"2026-04-01T12:40:59-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026amp;nbsp;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;Senior Clinical Trial Associate\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the Senior Clinical Trial Associate reporting to the Senior Manager, Clinical Trial Leader, you will provide comprehensive administrative and operational support to\u0026amp;nbsp;clinical team members across all study activities, including both in-house and outsourced trials. This role supports cross-functional study execution through coordination with internal teams, external vendors, and site staff, and may include contributing to study documentation such as informed consent forms (ICFs) and central IRB submissions, supporting site payments and other study-related operational activities, as well as liaising with and following up with investigator sites. Responsibilities include assisting with study start-up, maintenance, and closeout activities; managing study documentation and materials; supporting vendor management; and\u0026amp;nbsp;maintaining\u0026amp;nbsp;study trackers and financial records. This position adheres to Clinical Standard Operating Procedures and Good Clinical Practice (ICH) guidelines.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based out of either our office San Francisco or Cambridge office and will require approximately 10% travel.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Your work will\u0026amp;nbsp;\u0026lt;em\u0026gt;primarily\u0026lt;/em\u0026gt;\u0026amp;nbsp;encompass:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Supports the Clinical Trial Lead (CTL) and Study Execution Team (SET), ensuring ongoing\u0026amp;nbsp;accurate\u0026amp;nbsp;and essential documentation of study conduct\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manages study-related vendors and serves as a point of contact for contracted CROs, study staff, contract labs, and other study vendors\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Acts as a key point of contact for investigator sites, facilitating communication, and ensuring effective coordination of study-related activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conducts oversight of sample collection, shipment, and analyses\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conducts reconciliation and tracking of study processes in collaboration with study team and escalates issues in\u0026amp;nbsp;a timely\u0026amp;nbsp;fashion to study lead\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identifies\u0026amp;nbsp;potential risks and proactively resolves issues with CROs\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists\u0026amp;nbsp;in the development of vendor management and other study plans and compiles study and quality metrics for CTL, management, and/or team review(s)\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitates flow and maintenance of correspondence with vendors and sites to provide or obtain study-specific information\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensures receipt, completeness, accuracy, and\u0026amp;nbsp;appropriate filing\u0026amp;nbsp;(Trial Master File, study SharePoint, other\u0026amp;nbsp;study\u0026amp;nbsp;or Olema-specific systems) of clinical and administrative documents\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists\u0026amp;nbsp;in coordination of study initiation documentation materials, including support for central IRB submission documents and review of site-specific informed consent forms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinates electronic distribution and/or shipment of study-related materials, as appropriate\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborates with relevant team members in the coordination and tracking of vendor and investigator site contracts, budgets, invoices, and/or payments as needed\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contributes to the development of the TMF plan and conducts periodic quality control reviews and records reconciliation of the Trial Master File (TMF)\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs study and departmental administrative and clerical duties such as preparing agendas and minutes for team meetings and providing meeting planning and\u0026amp;nbsp;presentations\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actively\u0026amp;nbsp;participates\u0026amp;nbsp;in department initiatives and goals, providing suggestions that support the vision, mission, and enhancement of Clinical Operations; may lead certain SOPs or other processes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Ideal\u0026amp;nbsp;Candidate Profile\u0026amp;nbsp;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;A love of challenging, important work.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All\u0026amp;nbsp;employees\u0026amp;nbsp;within our company play a\u0026amp;nbsp;unique and\u0026amp;nbsp;crucial role\u0026amp;nbsp;in our success, both in\u0026amp;nbsp;accomplishing\u0026amp;nbsp;our mission and building\u0026amp;nbsp;a positive\u0026amp;nbsp;company culture. As such, we are looking for\u0026amp;nbsp;someone with\u0026amp;nbsp;the right combination of\u0026amp;nbsp;\u0026lt;em\u0026gt;knowledge\u0026lt;/em\u0026gt;,\u0026amp;nbsp;\u0026lt;em\u0026gt;experience\u0026lt;/em\u0026gt;, and\u0026amp;nbsp;\u0026lt;em\u0026gt;attributes\u0026lt;/em\u0026gt;\u0026amp;nbsp;for this role.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Knowledge\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree is\u0026amp;nbsp;required\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with FDA/EMA regulatory requirements and ICH/GCP guidelines is preferred\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of clinical protocols\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Experience\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 3\u0026amp;nbsp;years of related industry experience\u0026amp;nbsp;is\u0026amp;nbsp;required\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Senior CTA\u0026amp;nbsp;requires\u0026amp;nbsp;2 years\u0026#39; experience working as a Clinical Trial Associate.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency\u0026amp;nbsp;with Microsoft applications (e.g., Microsoft Word, Excel, PowerPoint, Outlook)\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with leading small group meetings and/or managing vendor relationships\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attributes\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Highly motivated and enjoys working in a fast-paced, dynamic environment\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent teamwork and collaboration skills\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Good organizational skills, ability to manage multiple tasks and meticulous attention to detail\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to accommodate a flexible work schedule according to clinical trial(s) priorities, as needed\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The base pay range for this position is expected to be \u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;$110,000 - $120,000\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;annually,\u0026amp;nbsp;however\u0026amp;nbsp;the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-CK1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4023657004,"name":"Clinical","child_ids":[],"parent_id":null}],"offices":[{"id":4008188004,"name":"Brannan / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4008187004,"name":"Owens / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4013948004,"name":"Rogers / Boston","location":"Boston, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5480105004","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":4876929004,"location":{"name":"San Francisco, California"},"metadata":null,"id":5480105004,"updated_at":"2026-04-09T11:59:07-04:00","requisition_id":"285","title":"Senior Director, Marketing","company_name":"Olema Oncology","first_published":"2026-04-01T10:18:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role \u0026amp;gt;\u0026amp;gt;\u0026amp;gt; Senior Director, Marketing\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the \u0026lt;strong\u0026gt;Senior Director, Marketing \u0026lt;/strong\u0026gt;you will design and execute the Commercial roadmap that enables the successful potential U.S. launch of palazestrant, Olema’s lead program currently in Phase 3 for ER+ HER2- metastatic breast cancer. The ideal candidate will have experience in the commercialization of oral oncology therapies in breast cancer and a track record of leading successful oncology drug launches in the US.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based out of our San Francisco office and will require travel as needed.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Your work will\u0026amp;nbsp;\u0026lt;em\u0026gt;primarily\u0026lt;/em\u0026gt; encompass:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Building the strategic marketing plan and leading launch readiness initiatives (branding, positioning, messaging platform, story flow and creative imagery) to deliver a successful palazestrant launch\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing, prioritizing, and implementing market development activities that deepen awareness of unmet needs and address knowledge gaps among customers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Designing the go-to-market approach that delivers resource-efficient customer engagement, customer behavior change and adoption at launch\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing KPIs to assess launch performance and analyzing market, customer, and competitor trends, incorporating insights into marketing strategies and plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establishing a strong relationship with Medical Affairs, and eventually, the Sales team and other field-based commercial teams to ensure optimal execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partnering cross-functionally with Clinical Development, Regulatory and other internal stakeholders to gather input for functional activities and ensure alignment with launch readiness activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Managing partner agency and vendor relationships and workflow\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensuring strategic and tactical plans meet compliance and regulatory guidelines and company policies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Delivering marketing operating expenses within budget\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Ideal Candidate Profile\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;A love of challenging, important work. \u0026lt;/strong\u0026gt;We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees within our company play a unique and crucial role in our success, both in accomplishing our mission and building a positive company culture. As such, we are looking for someone with the right combination of \u0026lt;em\u0026gt;knowledge\u0026lt;/em\u0026gt;, \u0026lt;em\u0026gt;experience\u0026lt;/em\u0026gt;, and \u0026lt;em\u0026gt;attributes\u0026lt;/em\u0026gt; for this role.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Knowledge:\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; MBA preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of customer adoption behavior in breast cancer\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of the laws and regulations regarding interactions with the healthcare community\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Experience:\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 8 years of progressive commercial experience at biotechnology and/or pharmaceutical companies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Successful history of developing and executing marketing strategy plans and leading the launch of new oncology products in the US\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to leverage insights and analytics to deliver impactful marketing strategies and tactics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to influence effectively across an organization at all levels\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience developing strategies to win in competitive markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience thriving in a small company environment, with a hands-on and pragmatic leadership style\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent prioritization skills to deliver results within reasonably established timelines\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Attributes:\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Team player and collaborative: puts success of team above own interests; supports everyone\u0026#39;s efforts to succeed; shares expertise with others\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possesses a get-the-job done attitude and identifies not just challenges but takes the initiative to identify solutions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analytical thinking with problem-solving skills and the ability to adapt to changing priorities and deadlines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written verbal and interpersonal communication skills and ability to adapt communication styles to varied internal and external partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Impeccable professional ethics, integrity, and judgment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The base pay range for this position is expected to be \u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;$250,000 - $285,000\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt; annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-AD1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4084524004,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4008187004,"name":"Owens / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5977366004","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":5144982004,"location":{"name":"San Francisco, California"},"metadata":null,"id":5977366004,"updated_at":"2026-04-22T19:37:24-04:00","requisition_id":"436","title":"Senior Manager, Legal Operations \u0026 Contracts","company_name":"Olema Oncology","first_published":"2026-04-22T19:37:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026amp;nbsp;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;Senior Manager,\u0026amp;nbsp;Legal Operations \u0026amp;amp; Contracts\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the\u0026amp;nbsp;\u0026lt;strong\u0026gt;Senior Manager,\u0026amp;nbsp;Legal Operations \u0026amp;amp; Contracts\u0026amp;nbsp;\u0026lt;/strong\u0026gt;reporting to the\u0026amp;nbsp;Vice-President, Legal\u0026amp;nbsp;Counsel,\u0026amp;nbsp;you will bring strong legal operations\u0026amp;nbsp;expertise, including process management, execution, compliance, and process optimization, with a focus on building and scaling efficient workflows. In addition, you bring a deep background in drafting, reviewing, and negotiating a high volume of both routine and complex contracts. This role will\u0026amp;nbsp;operate\u0026amp;nbsp;independently across functions as a trusted partner, proactively managing the end-to-end contract lifecycle for commercialization contracts while driving operational excellence and efficiency.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role\u0026amp;nbsp;will support the legal team through KPI tracking, metrics, and analysis, while\u0026amp;nbsp;identifying\u0026amp;nbsp;and driving workflow efficiencies as the function scales. This role requires strong legal knowledge, the ability to work independently, and to build and\u0026amp;nbsp;maintain\u0026amp;nbsp;cross-functional relationships. The ideal candidate is detail-oriented, highly organized, and proficient with systems and tools, with a solid understanding of corporate contracts.\u0026amp;nbsp;Strong communication, collaboration, and time management skills are essential, along with a proactive, positive, and growth-oriented mindset.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role\u0026amp;nbsp;is\u0026amp;nbsp;based out of our\u0026amp;nbsp;San Francisco or Boston\u0026amp;nbsp;office and will require\u0026amp;nbsp;10%\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;travel.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Your work will\u0026amp;nbsp;\u0026lt;em\u0026gt;primarily\u0026lt;/em\u0026gt;\u0026amp;nbsp;encompass:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage legal\u0026amp;nbsp;operations\u0026amp;nbsp;activities including contributing to the development of training materials, documentation, and process improvements to support efficient contracting practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and optimize legal operations processes such as contract management, document management, knowledge management, vendor relationships, and strategic processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive operational efficiencies through technology and process improvements, managing legal department projects, and support day-to-day operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement policies and procedures to improve legal department effectiveness and efficiency\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Negotiate, draft,\u0026amp;nbsp;review,\u0026amp;nbsp;and manage a wide range of contracts.\u0026amp;nbsp;(including confidentiality agreements, SOWs, consulting and service agreements, materials transfer agreements, sponsored research agreements, clinical study agreements, and various vendor services agreements) with guidance from senior attorneys as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate with internal stakeholders\u0026amp;nbsp;regarding\u0026amp;nbsp;contractual risks and support development of practical\u0026amp;nbsp;mitigation\u0026amp;nbsp;approaches\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure contractual terms and conditions are consistent with Olema policies, standards, and established guidance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with applicable laws and regulations, including data protection and privacy requirements\u0026amp;nbsp;(e.g., GDPR, HIPAA)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as an escalation point of contact for internal and external contract process/status questions and escalate more complex issues as appropriate\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage contract workflow and support adherence to contract turnaround timelines to ensure efficient execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support and partner in the development, enhancement, and maintenance of contract templates and SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Be the contract management systems expert (i.e. Agiloft)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with outside counsel and in-house legal team to obtain legal documents, e.g., patent declarations and assignments, and manage legal records\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Ideal\u0026amp;nbsp;Candidate Profile\u0026amp;nbsp;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;A love of challenging, important work.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All\u0026amp;nbsp;employees\u0026amp;nbsp;within our company play a\u0026amp;nbsp;unique and\u0026amp;nbsp;crucial role\u0026amp;nbsp;in our success, both in\u0026amp;nbsp;accomplishing\u0026amp;nbsp;our mission and building\u0026amp;nbsp;a positive\u0026amp;nbsp;company culture. As such, we are looking for\u0026amp;nbsp;someone with\u0026amp;nbsp;the right combination of\u0026amp;nbsp;\u0026lt;em\u0026gt;knowledge\u0026lt;/em\u0026gt;,\u0026amp;nbsp;\u0026lt;em\u0026gt;experience\u0026lt;/em\u0026gt;, and\u0026amp;nbsp;\u0026lt;em\u0026gt;attributes\u0026lt;/em\u0026gt;\u0026amp;nbsp;for this role.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Knowledge:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s Degree,\u0026amp;nbsp;is\u0026amp;nbsp;required\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paralegal certificate or legal studies background preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience leading legal operations, including contract lifecycle management, process optimization, and implementation of tools and systems to improve efficiency\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Managing full contract lifecycle, including drafting, negotiating, editing, and execution, with a strong understanding of contract terms, structure, and end-to-end contract management processes (tracking, approval, and execution)\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge or experience with paralegal support tasks, with a focus on compliance program matter, contract or corporate matters\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of the drug discovery and development process and ability to understand risks and requirements associated with pharmaceutical contracting preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency\u0026amp;nbsp;with contract management software\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Experience:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;A minimum of seven years\u0026amp;nbsp;(7+)\u0026amp;nbsp;of relevant experience in\u0026amp;nbsp;legal operations and contract management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-house experience at a biotechnology, pharmaceutical or life science\u0026amp;nbsp;company with\u0026amp;nbsp;a focus on\u0026amp;nbsp;legal operations and\u0026amp;nbsp;agreement drafting and negotiation,\u0026amp;nbsp;strongly\u0026amp;nbsp;preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience working with attorneys and senior leaders across various functions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work both independently and effectively across a variety of functional groups (such as Commercial, Research and Development, CMC, Human Resources, Finance, Facilities and IT) and all levels of management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Liaison and point of contact for business contract owners and vendor/agency inquiries related to contracting and payment in partnership with legal, finance, and procurement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong technical skills (e.g., Microsoft Word, Excel and PowerPoint, Contract Management Systems, Docusign)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Attributes:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Highly organized, detail-oriented, and process driven\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive and solutions-oriented\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong collaborator with the ability to influence cross-functional teams\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable operating in a growing, fast-paced biotech environment\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High level\u0026amp;nbsp;of integrity and discretion\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible and willing to learn new procedures and skill sets\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The base pay range for this position is expected to be \u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;$150,000 - $170,000\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;annually;\u0026amp;nbsp;however,\u0026amp;nbsp;the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-MT1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4023658004,"name":"Business and Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4008187004,"name":"Owens / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4013948004,"name":"Rogers / Boston","location":"Boston, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5977367004","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":5144982004,"location":{"name":"Boston, Massachusetts"},"metadata":null,"id":5977367004,"updated_at":"2026-04-22T19:37:25-04:00","requisition_id":"436","title":"Senior Manager, Legal Operations \u0026 Contracts","company_name":"Olema Oncology","first_published":"2026-04-22T19:37:25-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026amp;nbsp;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;Senior Manager,\u0026amp;nbsp;Legal Operations \u0026amp;amp; Contracts\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the\u0026amp;nbsp;\u0026lt;strong\u0026gt;Senior Manager,\u0026amp;nbsp;Legal Operations \u0026amp;amp; Contracts\u0026amp;nbsp;\u0026lt;/strong\u0026gt;reporting to the\u0026amp;nbsp;Vice-President, Legal\u0026amp;nbsp;Counsel,\u0026amp;nbsp;you will bring strong legal operations\u0026amp;nbsp;expertise, including process management, execution, compliance, and process optimization, with a focus on building and scaling efficient workflows. In addition, you bring a deep background in drafting, reviewing, and negotiating a high volume of both routine and complex contracts. This role will\u0026amp;nbsp;operate\u0026amp;nbsp;independently across functions as a trusted partner, proactively managing the end-to-end contract lifecycle for commercialization contracts while driving operational excellence and efficiency.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role\u0026amp;nbsp;will support the legal team through KPI tracking, metrics, and analysis, while\u0026amp;nbsp;identifying\u0026amp;nbsp;and driving workflow efficiencies as the function scales. This role requires strong legal knowledge, the ability to work independently, and to build and\u0026amp;nbsp;maintain\u0026amp;nbsp;cross-functional relationships. The ideal candidate is detail-oriented, highly organized, and proficient with systems and tools, with a solid understanding of corporate contracts.\u0026amp;nbsp;Strong communication, collaboration, and time management skills are essential, along with a proactive, positive, and growth-oriented mindset.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role\u0026amp;nbsp;is\u0026amp;nbsp;based out of our\u0026amp;nbsp;San Francisco or Boston\u0026amp;nbsp;office and will require\u0026amp;nbsp;10%\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;travel.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Your work will\u0026amp;nbsp;\u0026lt;em\u0026gt;primarily\u0026lt;/em\u0026gt;\u0026amp;nbsp;encompass:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage legal\u0026amp;nbsp;operations\u0026amp;nbsp;activities including contributing to the development of training materials, documentation, and process improvements to support efficient contracting practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and optimize legal operations processes such as contract management, document management, knowledge management, vendor relationships, and strategic processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive operational efficiencies through technology and process improvements, managing legal department projects, and support day-to-day operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement policies and procedures to improve legal department effectiveness and efficiency\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Negotiate, draft,\u0026amp;nbsp;review,\u0026amp;nbsp;and manage a wide range of contracts.\u0026amp;nbsp;(including confidentiality agreements, SOWs, consulting and service agreements, materials transfer agreements, sponsored research agreements, clinical study agreements, and various vendor services agreements) with guidance from senior attorneys as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate with internal stakeholders\u0026amp;nbsp;regarding\u0026amp;nbsp;contractual risks and support development of practical\u0026amp;nbsp;mitigation\u0026amp;nbsp;approaches\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure contractual terms and conditions are consistent with Olema policies, standards, and established guidance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with applicable laws and regulations, including data protection and privacy requirements\u0026amp;nbsp;(e.g., GDPR, HIPAA)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as an escalation point of contact for internal and external contract process/status questions and escalate more complex issues as appropriate\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage contract workflow and support adherence to contract turnaround timelines to ensure efficient execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support and partner in the development, enhancement, and maintenance of contract templates and SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Be the contract management systems expert (i.e. Agiloft)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with outside counsel and in-house legal team to obtain legal documents, e.g., patent declarations and assignments, and manage legal records\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Ideal\u0026amp;nbsp;Candidate Profile\u0026amp;nbsp;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;A love of challenging, important work.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All\u0026amp;nbsp;employees\u0026amp;nbsp;within our company play a\u0026amp;nbsp;unique and\u0026amp;nbsp;crucial role\u0026amp;nbsp;in our success, both in\u0026amp;nbsp;accomplishing\u0026amp;nbsp;our mission and building\u0026amp;nbsp;a positive\u0026amp;nbsp;company culture. As such, we are looking for\u0026amp;nbsp;someone with\u0026amp;nbsp;the right combination of\u0026amp;nbsp;\u0026lt;em\u0026gt;knowledge\u0026lt;/em\u0026gt;,\u0026amp;nbsp;\u0026lt;em\u0026gt;experience\u0026lt;/em\u0026gt;, and\u0026amp;nbsp;\u0026lt;em\u0026gt;attributes\u0026lt;/em\u0026gt;\u0026amp;nbsp;for this role.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Knowledge:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s Degree,\u0026amp;nbsp;is\u0026amp;nbsp;required\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paralegal certificate or legal studies background preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience leading legal operations, including contract lifecycle management, process optimization, and implementation of tools and systems to improve efficiency\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Managing full contract lifecycle, including drafting, negotiating, editing, and execution, with a strong understanding of contract terms, structure, and end-to-end contract management processes (tracking, approval, and execution)\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge or experience with paralegal support tasks, with a focus on compliance program matter, contract or corporate matters\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of the drug discovery and development process and ability to understand risks and requirements associated with pharmaceutical contracting preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency\u0026amp;nbsp;with contract management software\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Experience:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;A minimum of seven years\u0026amp;nbsp;(7+)\u0026amp;nbsp;of relevant experience in\u0026amp;nbsp;legal operations and contract management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-house experience at a biotechnology, pharmaceutical or life science\u0026amp;nbsp;company with\u0026amp;nbsp;a focus on\u0026amp;nbsp;legal operations and\u0026amp;nbsp;agreement drafting and negotiation,\u0026amp;nbsp;strongly\u0026amp;nbsp;preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience working with attorneys and senior leaders across various functions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work both independently and effectively across a variety of functional groups (such as Commercial, Research and Development, CMC, Human Resources, Finance, Facilities and IT) and all levels of management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Liaison and point of contact for business contract owners and vendor/agency inquiries related to contracting and payment in partnership with legal, finance, and procurement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong technical skills (e.g., Microsoft Word, Excel and PowerPoint, Contract Management Systems, Docusign)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Attributes:\u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Highly organized, detail-oriented, and process driven\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive and solutions-oriented\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong collaborator with the ability to influence cross-functional teams\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable operating in a growing, fast-paced biotech environment\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High level\u0026amp;nbsp;of integrity and discretion\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible and willing to learn new procedures and skill sets\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The base pay range for this position is expected to be \u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;$150,000 - $170,000\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;annually;\u0026amp;nbsp;however,\u0026amp;nbsp;the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-MT1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4023658004,"name":"Business and Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4008187004,"name":"Owens / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4013948004,"name":"Rogers / Boston","location":"Boston, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5841388004","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":5070520004,"location":{"name":"San Francisco, California"},"metadata":null,"id":5841388004,"updated_at":"2026-04-10T12:59:42-04:00","requisition_id":"417","title":"Vice President, Market Access","company_name":"Olema Oncology","first_published":"2026-04-01T09:27:39-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role \u0026amp;gt;\u0026amp;gt;\u0026amp;gt; Vice President, Market Access\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the Vice President of Market Access, you will build and lead the market access organization and capabilities critical to Olema’s mission to bring better medicines to breast cancer patients. This leader will have a significant role in preparing the company and the market for the launch of Olema’s lead product, palazestrant, a novel SERD/CERAN being evaluated in ER+ HER2- metastatic breast cancer.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The leadership scope spans all aspects of U.S. market access—payor and account engagement, pricing, coverage and reimbursement, distribution, and patient support programs. The ideal candidate brings deep market access expertise in oral oncology therapeutics and has demonstrated success building infrastructure from the ground up, delivering value in competitive markets, and thriving in a fast-paced, resource-conscious biotech environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based out of our San Francisco, CA or Boston, MA office and will require travel as needed.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Your work will primarily encompass:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Establishing the infrastructure and capabilities needed to support the potential US launch of palazestrant\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing and executing strategy across payor and account access, pricing, coverage and reimbursement, trade and distribution, and patient support\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing payer value propositions and evidence plans that support coverage and adoption\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leading payor and account engagement across all relevant channels\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Shaping pricing and contracting strategy, including gross-to-net considerations and channel strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Setting up and managing trade and distribution strategy, including specialty pharmacy and specialty distributor network design and partner selection\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Building patient support programs that reduce barriers for patients and providers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partnering cross-functionally with Marketing, Commercial Strategy and Operations, Sales, Medical Affairs, Regulatory, Finance, Legal, Manufacturing, and Supply Chain\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Building and mentoring a high-performing team in a fast-paced, growing biotech environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Ideal Candidate Profile\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;A love of challenging, important work. We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees within our company play a unique and crucial role in our success, both in accomplishing our mission and building a positive company culture. As such, we are looking for someone with the right combination of knowledge, experience, and attributes for this role.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Knowledge\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; advanced degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of US payor, pricing, reimbursement, specialty pharmacy, and distribution dynamics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep expertise in oncology market access, specifically for oral therapeutics\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Experience\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 15+ years of biopharmaceutical experience, including significant market access leadership experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success building market access team and infrastructure in a first-time launching company or similar pre-commercial biotech setting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience developing strategies to win in competitive markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience thriving in a small company environment, with a hands-on and pragmatic leadership style\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attributes\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Team player and collaborative: puts success of team above own interests; supports everyone\u0026#39;s efforts to succeed; shares expertise with others\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;People developer: balances team and individual responsibilities; gives and welcomes feedback\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possesses a get-the-job done attitude and identifies not just challenges but takes the initiative to identify solutions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analytical thinking with problem-solving skills and the ability to adapt to changing priorities and deadlines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written verbal and interpersonal communication skills and ability to adapt communication styles to varied internal and external partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Impeccable professional ethics, integrity, and judgment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The base pay range for this position is expected to be \u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;$300,000 - $350,000\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt;\u0026amp;nbsp;\u0026lt;/em\u0026gt;annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-AD1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4084524004,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4008187004,"name":"Owens / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5977235004","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":5144908004,"location":{"name":"Boston, Massachusetts"},"metadata":null,"id":5977235004,"updated_at":"2026-04-21T16:01:06-04:00","requisition_id":"435","title":"Vice President Quality Assurance","company_name":"Olema Oncology","first_published":"2026-04-21T13:39:48-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026amp;nbsp;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;Vice President, Quality\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Assurance\u0026lt;/strong\u0026gt; \u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The\u0026amp;nbsp;\u0026lt;strong\u0026gt;Vice President, Quality Assurance\u0026lt;/strong\u0026gt; serves as the senior leader accountable for defining and driving Olema’s global quality strategy, systems, and governance across the full product lifecycle, including clinical development, manufacturing, pharmacovigilance, and commercial. This leader is the primary voice of Quality at the executive level and\u0026amp;nbsp;ensures a phase-appropriate, risk-based approach to quality that reflects the needs of oncology drug development, where patient safety, data integrity, and speed are critical. \u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;118\u0026quot; data-end=\u0026quot;435\u0026quot;\u0026gt;Operating with appropriate independence, this role partners cross-functionally and leads an established Quality leadership team across GCP, GMP, and GPV - aligning priorities, strengthening execution, and ensuring inspection readiness as Olema advances toward late-stage development.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role\u0026amp;nbsp;is\u0026amp;nbsp;based out of our\u0026amp;nbsp;either our San Francisco, CA or Boston, MA\u0026amp;nbsp;office and will require\u0026amp;nbsp;some travel as needed.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As \u0026lt;strong\u0026gt;Vice President, Quality Assurance\u0026lt;/strong\u0026gt;, your work will\u0026amp;nbsp;\u0026lt;em\u0026gt;primarily\u0026lt;/em\u0026gt; encompass:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Quality Strategy \u0026amp;amp; Leadership\u0026lt;/strong\u0026gt; \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Define and drive a pragmatic, phase-appropriate and unified Quality strategy aligned with Olema’s pipeline and corporate objectives  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the senior Quality leader, establishing clear governance, decision-making frameworks, and escalation pathways  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and develop Quality leadership across GCP, GMP, and GPV, enabling strong execution and maintaining clear accountability  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster a culture of quality, integrity, and patient focus across the organization  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as escalation point for significant quality, compliance, and patient safety risks  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure ongoing inspection readiness across clinical, manufacturing, and safety domains \u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Quality Systems \u0026amp;amp; Governance\u0026lt;/strong\u0026gt; \u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Set expectations and direction for a scalable, integrated, and sustainable Quality Management framework spanning clinical through commercial stages  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure effectiveness and evolution of Quality systems through oversight of functional leaders across the QA function  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive consistency in quality processes, risk management approaches, and data integrity standards across the organization  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish clear quality metrics and reporting to enable risk visibility and informed decision-making \u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Clinical Quality (GCP)\u0026lt;/strong\u0026gt; \u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure Quality approaches appropriately support the execution of oncology clinical trials  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide oversight of clinical quality and CRO management to ensure patient safety and data integrity  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Clinical and Regulatory to support inspection-ready programs and submissions\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Manufacturing \u0026amp;amp; Commercial Readiness (GMP)\u0026lt;/strong\u0026gt; \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure Quality strategy supports manufacturing scale-up and readiness for late-stage development and commercialization  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee GMP Quality through established leadership, ensuring appropriate CMO/CDMO oversight and inspection preparedness  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide Quality input into CMC, validation, and supply chain readiness activities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Pharmacovigilance Quality (GPV)\u0026lt;/strong\u0026gt; \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee the pharmacovigilance quality framework, ensuring compliance, data integrity, and effective safety surveillance  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure PV systems and vendors are appropriately governed and inspection-ready  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner cross-functionally to support ongoing evaluation of benefit-risk\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Inspection, Audit \u0026amp;amp; Risk Management\u0026lt;/strong\u0026gt; \u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the Company’s approach to regulatory inspections, including preparation and execution  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure risk-based audit programs across GCP, GMP, and GPV  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive proactive identification and mitigation of quality and compliance risks\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Cross-Functional Leadership\u0026lt;/strong\u0026gt; \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with Executive Leadership, Regulatory, Clinical, and Manufacturing, to embed quality across the organization  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide clear, actionable Quality perspectives to support business decisions  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Quality in executive discussions and external engagements as needed  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Ideal Candidate Profile \u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;A love of challenging, important work.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All\u0026amp;nbsp;employees\u0026amp;nbsp;within our company play a\u0026amp;nbsp;unique and\u0026amp;nbsp;crucial role\u0026amp;nbsp;in our success, both in\u0026amp;nbsp;accomplishing\u0026amp;nbsp;our mission and building\u0026amp;nbsp;a positive\u0026amp;nbsp;company culture. As such, we are looking for\u0026amp;nbsp;someone with\u0026amp;nbsp;the right combination of\u0026amp;nbsp;\u0026lt;em\u0026gt;knowledge\u0026lt;/em\u0026gt;,\u0026amp;nbsp;\u0026lt;em\u0026gt;experience\u0026lt;/em\u0026gt;, and\u0026amp;nbsp;\u0026lt;em\u0026gt;attributes\u0026lt;/em\u0026gt;\u0026amp;nbsp;for this role.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Knowledge\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree in Life Sciences or related discipline (PhD, PharmD, MS)\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep knowledge of FDA, EMA, ICH, and global\u0026amp;nbsp;GxP\u0026amp;nbsp;and pharmacovigilance (GPV) regulatory requirement\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise\u0026amp;nbsp;across GCP, GMP, and GPV Quality domains\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of Quality systems, governance, and inspection readiness practices\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of oncology drug development\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Experience\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 15+ years of Quality experience in biotech/pharma\u0026amp;nbsp;with increasing scope and responsibility\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Significant people management and leadership experience, including leading senior team members\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience overseeing global vendor networks, including CROs, CMOs, CDMOs, and PV vendors\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience across GCP, GMP, and GPV environments\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven\u0026amp;nbsp;track record\u0026amp;nbsp;supporting programs from clinical development through late-stage or commercial readiness\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience leading regulatory inspections and interacting with global health authorities\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience implementing and\u0026amp;nbsp;maintaining\u0026amp;nbsp;Quality systems and compliance frameworks\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Attributes\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong leadership capability with ability to lead through and develop senior leaders\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective communicator with executive presence and influencing skills\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sound judgment and decision-making in complex, risk-based environments\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to\u0026amp;nbsp;operate\u0026amp;nbsp;effectively in a fast-paced, evolving biotech environment\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to quality, compliance, and patient safety\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The base pay range for this position is expected to be \u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;$315,000 - $340,000\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt; annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-AD1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4023657004,"name":"Clinical","child_ids":[],"parent_id":null}],"offices":[{"id":4008188004,"name":"Brannan / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4008187004,"name":"Owens / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4013948004,"name":"Rogers / Boston","location":"Boston, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/olema/jobs/5977234004","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":5144908004,"location":{"name":"San Francisco, California"},"metadata":null,"id":5977234004,"updated_at":"2026-04-21T16:01:36-04:00","requisition_id":"435","title":"Vice President, Quality Assurance","company_name":"Olema Oncology","first_published":"2026-04-21T13:39:49-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for \u0026lt;strong\u0026gt;our patients, for your career, for what’s beyond\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You can view our latest corporate deck and other presentations \u0026lt;a href=\u0026quot;https://ir.olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;here\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026amp;nbsp;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;Vice President, Quality\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Assurance\u0026lt;/strong\u0026gt; \u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The\u0026amp;nbsp;\u0026lt;strong\u0026gt;Vice President, Quality Assurance\u0026lt;/strong\u0026gt; serves as the senior leader accountable for defining and driving Olema’s global quality strategy, systems, and governance across the full product lifecycle, including clinical development, manufacturing, pharmacovigilance, and commercial. This leader is the primary voice of Quality at the executive level and\u0026amp;nbsp;ensures a phase-appropriate, risk-based approach to quality that reflects the needs of oncology drug development, where patient safety, data integrity, and speed are critical. \u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;118\u0026quot; data-end=\u0026quot;435\u0026quot;\u0026gt;Operating with appropriate independence, this role partners cross-functionally and leads an established Quality leadership team across GCP, GMP, and GPV - aligning priorities, strengthening execution, and ensuring inspection readiness as Olema advances toward late-stage development.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role\u0026amp;nbsp;is\u0026amp;nbsp;based out of our\u0026amp;nbsp;either our San Francisco, CA or Boston, MA\u0026amp;nbsp;office and will require\u0026amp;nbsp;some travel as needed.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As \u0026lt;strong\u0026gt;Vice President, Quality Assurance\u0026lt;/strong\u0026gt;, your work will\u0026amp;nbsp;\u0026lt;em\u0026gt;primarily\u0026lt;/em\u0026gt; encompass:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Quality Strategy \u0026amp;amp; Leadership\u0026lt;/strong\u0026gt; \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Define and drive a pragmatic, phase-appropriate and unified Quality strategy aligned with Olema’s pipeline and corporate objectives  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the senior Quality leader, establishing clear governance, decision-making frameworks, and escalation pathways  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and develop Quality leadership across GCP, GMP, and GPV, enabling strong execution and maintaining clear accountability  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster a culture of quality, integrity, and patient focus across the organization  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as escalation point for significant quality, compliance, and patient safety risks  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure ongoing inspection readiness across clinical, manufacturing, and safety domains \u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Quality Systems \u0026amp;amp; Governance\u0026lt;/strong\u0026gt; \u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Set expectations and direction for a scalable, integrated, and sustainable Quality Management framework spanning clinical through commercial stages  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure effectiveness and evolution of Quality systems through oversight of functional leaders across the QA function  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive consistency in quality processes, risk management approaches, and data integrity standards across the organization  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish clear quality metrics and reporting to enable risk visibility and informed decision-making \u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Clinical Quality (GCP)\u0026lt;/strong\u0026gt; \u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure Quality approaches appropriately support the execution of oncology clinical trials  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide oversight of clinical quality and CRO management to ensure patient safety and data integrity  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Clinical and Regulatory to support inspection-ready programs and submissions\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Manufacturing \u0026amp;amp; Commercial Readiness (GMP)\u0026lt;/strong\u0026gt; \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure Quality strategy supports manufacturing scale-up and readiness for late-stage development and commercialization  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee GMP Quality through established leadership, ensuring appropriate CMO/CDMO oversight and inspection preparedness  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide Quality input into CMC, validation, and supply chain readiness activities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Pharmacovigilance Quality (GPV)\u0026lt;/strong\u0026gt; \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee the pharmacovigilance quality framework, ensuring compliance, data integrity, and effective safety surveillance  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure PV systems and vendors are appropriately governed and inspection-ready  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner cross-functionally to support ongoing evaluation of benefit-risk\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Inspection, Audit \u0026amp;amp; Risk Management\u0026lt;/strong\u0026gt; \u0026lt;/em\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the Company’s approach to regulatory inspections, including preparation and execution  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure risk-based audit programs across GCP, GMP, and GPV  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive proactive identification and mitigation of quality and compliance risks\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Cross-Functional Leadership\u0026lt;/strong\u0026gt; \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with Executive Leadership, Regulatory, Clinical, and Manufacturing, to embed quality across the organization  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide clear, actionable Quality perspectives to support business decisions  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Quality in executive discussions and external engagements as needed  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Ideal Candidate Profile \u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;A love of challenging, important work.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All\u0026amp;nbsp;employees\u0026amp;nbsp;within our company play a\u0026amp;nbsp;unique and\u0026amp;nbsp;crucial role\u0026amp;nbsp;in our success, both in\u0026amp;nbsp;accomplishing\u0026amp;nbsp;our mission and building\u0026amp;nbsp;a positive\u0026amp;nbsp;company culture. As such, we are looking for\u0026amp;nbsp;someone with\u0026amp;nbsp;the right combination of\u0026amp;nbsp;\u0026lt;em\u0026gt;knowledge\u0026lt;/em\u0026gt;,\u0026amp;nbsp;\u0026lt;em\u0026gt;experience\u0026lt;/em\u0026gt;, and\u0026amp;nbsp;\u0026lt;em\u0026gt;attributes\u0026lt;/em\u0026gt;\u0026amp;nbsp;for this role.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Knowledge\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree in Life Sciences or related discipline (PhD, PharmD, MS)\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep knowledge of FDA, EMA, ICH, and global\u0026amp;nbsp;GxP\u0026amp;nbsp;and pharmacovigilance (GPV) regulatory requirement\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise\u0026amp;nbsp;across GCP, GMP, and GPV Quality domains\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of Quality systems, governance, and inspection readiness practices\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of oncology drug development\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Experience\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 15+ years of Quality experience in biotech/pharma\u0026amp;nbsp;with increasing scope and responsibility\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Significant people management and leadership experience, including leading senior team members\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience overseeing global vendor networks, including CROs, CMOs, CDMOs, and PV vendors\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience across GCP, GMP, and GPV environments\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven\u0026amp;nbsp;track record\u0026amp;nbsp;supporting programs from clinical development through late-stage or commercial readiness\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience leading regulatory inspections and interacting with global health authorities\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience implementing and\u0026amp;nbsp;maintaining\u0026amp;nbsp;Quality systems and compliance frameworks\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Attributes\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong leadership capability with ability to lead through and develop senior leaders\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective communicator with executive presence and influencing skills\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sound judgment and decision-making in complex, risk-based environments\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to\u0026amp;nbsp;operate\u0026amp;nbsp;effectively in a fast-paced, evolving biotech environment\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to quality, compliance, and patient safety\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The base pay range for this position is expected to be \u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;$315,000 - $340,000\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt; annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;visibility: hidden;\u0026quot;\u0026gt;#LI-AD1\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Important Information \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;gt;\u0026amp;gt;\u0026amp;gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We provide \u0026lt;strong\u0026gt;equal opportunity to all employees and applicants for employment\u0026lt;/strong\u0026gt; and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a \u0026lt;strong\u0026gt;competitive compensation and benefits package\u0026lt;/strong\u0026gt;, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;: \u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;We are aware of employment scams where individuals pose as representatives of Olema Oncology\u0026amp;nbsp;and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;a6e0c82d-5429-4e8c-b591-752f2a6a6de4\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;0\u0026quot;\u0026gt;olema.com\u0026lt;/a\u0026gt;; our careers page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://olema.com/careers/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;d0a0a54e-53bc-4d3b-adf5-ae9c7e616cf0\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;1\u0026quot;\u0026gt;olema.com/careers\u0026lt;/a\u0026gt;; our LinkedIn page is\u0026amp;nbsp;\u0026lt;a class=\u0026quot;x_Hyperlink x_SCXW164988465 x_BCX0\u0026quot; href=\u0026quot;https://www.linkedin.com/company/olema-oncology/\u0026quot; target=\u0026quot;_blank\u0026quot; data-outlook-id=\u0026quot;3d87665c-af14-40dc-bd98-9c9a4d15c43a\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;linkedin.com/company/olema-oncology\u0026lt;/a\u0026gt;.\u0026amp;nbsp;Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments\u0026amp;nbsp;of any kind, and does not make job offers without an in-person interview.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4023657004,"name":"Clinical","child_ids":[],"parent_id":null}],"offices":[{"id":4008188004,"name":"Brannan / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4008187004,"name":"Owens / SF","location":"San Francisco, California, United States","child_ids":[],"parent_id":null},{"id":4013948004,"name":"Rogers / Boston","location":"Boston, Massachusetts, United States","child_ids":[],"parent_id":null}]}],"meta":{"total":15}}