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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Senior Director, Clinical Data Management - **Company:** Bristol Myers Squibb - **Location:** San Diego, CA, United States - **Experience:** Expert - **Salary:** $261,110.0 - $316,404.0 - **Contract:** Permanent contract - **Skills:** Artificial Intelligence, Clinical Data Management, Databases, Data Cleansing, Data Governance, Data Integrity, Data Structures, Data Strategy, Information Technology, Data Management, Veeva - **Published:** July 19, 2026 - **Apply:** https://www.juju.com/job/00000000ghxg1q ## About the Role + 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 related field required. + Minimum of 12 years data management experience in pharmaceutical/biotech/CRO industry. + Demonstrated experience in team leadership and management. Ability to guide, mentor, and develop team members. + In-depth experience in the Oncology therapeutic area is required. + Proven ability to manage CRO relationships and oversee data management deliverables. + Experience utilizing AI-enabled tools to improve productivity and work efficiency. Preferred Requirements: + Experience with Veeva EDC system + Radiopharmaceutical experience preferred. ## Description 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., + Lead and oversee data management activities across the clinical portfolio, ensuring high-quality, timely, and compliant data deliverables for all studies + Provide strategic leadership for data management in support of NDA submissions, including database lock, submission readiness, and regulatory inspection preparedness + Build, lead, and develop the data management team, including hiring, performance management, and capability development + Serve as the primary interface with external partners to ensure alignment on data standards, processes and resource planning + Oversee vendor strategy and performance across all studies, including selection, budget management, timeline oversight, and quality assurance + Drive standardization of data management processes and lead development and implementation of SOPs to support scalable and inspection-ready operations + Establish and maintain efficient database build, data cleaning, and data review processes across studies, ensuring consistency and quality + Lead database strategy, including build, validation, and lock processes across studies, ensuring timely and high-quality delivery + Partner cross-functionally with Clinical Operations, Clinical Development, Biostatistics, and Safety to ensure alignment on study execution and data quality ## Related Videos - [Blueprints for Success: Steering a Global Data & AI Architecture](https://www.wearedevelopers.com/videos/1577-blueprints-for-success-steering-a-global-data-ai-architecture) - [Hacking Your Vacation: Using Data for Fun](https://www.wearedevelopers.com/videos/585-hacking-your-vacation-using-data-for-fun) - [Kubernetes and Microservices with Multi-Model Databases](https://www.wearedevelopers.com/videos/382-kubernetes-and-microservices-with-multi-model-databases) - [Big Business, Big Barriers? 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