Senior Director, Clinical Data Management
San Diego, CAPosted Jul 17, 2026
Career Areas Career Stories Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Careers Home Life at BMS Career Areas Student Opportunities Events How We Recruit Career Stories Search this site Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Single PositionView All JobsSenior Director, Clinical Data ManagementRemote - United StatesApply NowFind out how well you match with this jobUpload your resumeJob descriptionLife at BMSAt RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: https://careers.bms.com/rayzebio/The Senior Director, Head of Data Management, will lead data management activities for clinical development. This role is critical in establishing and managing data management strategy, ensuring high-quality database build, data integrity, and inspection readiness to support pivotal studies and regulatory submissions.The Senior Director will provide leadership across studies and programs, collaborating cross-functionally to ensure aligned data strategies, while driving efficiencies through process standardization, SOP development, vendor oversight, and implementation of automation and advanced technologies.Job ResponsibilitiesLead and oversee data management activities across the clinical portfolio, ensuring high-quality, timely, and compliant data deliverables for all studiesProvide strategic leadership for data management in support of NDA submissions, including database lock, submission readiness, and regulatory inspection preparednessBuild, lead, and develop the data management team, including hiring, performance management, and capability developmentServe as the primary interface with external partners to ensure alignment on data standards, processes and resource planningOversee vendor strategy and performance across all studies, including selection, budget management, timeline oversight, and quality assuranceDrive standardization of data management processes and lead development and implementation of SOPs to support scalable and inspection-ready operationsEstablish and maintain efficient database build, data cleaning, and data review processes across studies, ensuring consistency and qualityLead database strategy, including build, validation, and lock processes across studies, ensuring timely and high-quality deliveryPartner cross-functionally with Clinical Operations, Clinical Development, Biostatistics, and Safety to ensure alignment on study execution and data qualitySkills and Knowledge:Strong knowledge and experience of EDC systems (Medidata RAVE or Veeva).Solid knowledge of GCP, CDISC/CDASH data structures, ICH guidelines and FDA regulations.Excellent verbal and written communication skills.Strong analytical and problem-solving abilities. Basic Requirements:Bachelor’s or Master’s degree in Life Sciences, Computer Science, Mathematics, Health Sciences, or a...