Director, Clinical Data Management
Bristol Myers Squibb
August 30, 2026
Remote
United States
Clinical Research and Development
Director, Clinical Data Management
Summary
- Serve as the Clinical Data Management program lead for a new product, providing end-to-end data management leadership across clinical studies.
Job Responsibilities
- Lead data management from study start-up through database lock for the program and its individual studies.
- Develop and drive the data management strategy: start-up planning, database build oversight, data review approach, risk management, database lock, and submission readiness.
- Ensure high-quality, timely, decision-ready clinical trial data across studies.
- Oversee CROs and data management vendors to ensure clear expectations, quality, compliance, and timeline adherence.
- Partner cross-functionally with Biostatistics, Statistical Programming, Clinical Operations, Medical Monitoring, Safety, Regulatory Affairs, and others.
- Lead cross-functional data review activities; identify, escalate, and resolve data issues, trends, risks, and quality concerns.
- Oversee/contribute to key documentation (Data Management Plans, edit check specs, validation/reconciliation plans, data transfer agreements, data review plans, database lock documentation).
- Travel ~10%; evening/weekend work may be required.
- Leverage AI to drive performance through prioritization and scaled adoption.
Skills and Knowledge
- EDC systems: Medidata RAVE or Veeva.
- GCP; CDISC/CDASH data structures; ICH guidelines; FDA regulations.
- Strong communication; analytical and problem-solving skills.
Basic Requirements
- Bachelor’s or Master’s in Life Sciences, Computer Science, Mathematics, Health Sciences, or related field.
- 10+ years data management experience in pharma/biotech/CRO.
- Experience leading study teams/vendors or reports; ability to mentor.
- In-depth oncology therapeutic area experience.
- Proven ability to manage CRO relationships and oversee deliverables.
- Experience using AI-enabled tools.
Preferred Requirements
- Radiopharmaceutical experience.
Application Instructions
- Apply for requisition R1604965: Director, Clinical Data Management.
Summary
- Serve as the Clinical Data Management program lead for a new product, providing end-to-end data management leadership across clinical studies.
Job Responsibilities
- Lead data management from study start-up through database lock for the program and its individual studies.
- Develop and drive the data management strategy: start-up planning, database build oversight, data review approach, risk management, database lock, and submission readiness.
- Ensure high-quality, timely, decision-ready clinical trial data across studies.
- Oversee CROs and data management vendors to ensure clear expectations, quality, compliance, and timeline adherence.
- Partner cross-functionally with Biostatistics, Statistical Programming, Clinical Operations, Medical Monitoring, Safety, Regulatory Affairs, and others.
- Lead cross-functional data review activities; identify, escalate, and resolve data issues, trends, risks, and quality concerns.
- Oversee/contribute to key documentation (Data Management Plans, edit check specs, validation/reconciliation plans, data transfer agreements, data review plans, database lock documentation).
- Travel ~10%; evening/weekend work may be required.
- Leverage AI to drive performance through prioritization and scaled adoption.
Skills and Knowledge
- EDC systems: Medidata RAVE or Veeva.
- GCP; CDISC/CDASH data structures; ICH guidelines; FDA regulations.
- Strong communication; analytical and problem-solving skills.
Basic Requirements
- Bachelor’s or Master’s in Life Sciences, Computer Science, Mathematics, Health Sciences, or related field.
- 10+ years data management experience in pharma/biotech/CRO.
- Experience leading study teams/vendors or reports; ability to mentor.
- In-depth oncology therapeutic area experience.
- Proven ability to manage CRO relationships and oversee deliverables.
- Experience using AI-enabled tools.
Preferred Requirements
- Radiopharmaceutical experience.
Application Instructions
- Apply for requisition R1604965: Director, Clinical Data Management.