Senior Director, Clinical Data Management
Bristol Myers Squibb
August 11, 2026
Remote
United States
Clinical Research and Development
Job Responsibilities
- Lead and oversee data management activities across the clinical portfolio, ensuring high-quality, timely, compliant data deliverables.
- Provide strategic leadership for data management in support of NDA submissions (database lock, submission readiness, inspection preparedness).
- Build, lead, and develop the data management team (hiring, performance management, capability development).
- Serve as primary interface with external partners to align on data standards, processes, and resourcing.
- Oversee vendor strategy/performance (selection, budget, timeline oversight, quality assurance).
- Standardize data management processes; develop and implement SOPs for scalable, inspection-ready operations.
- Establish and maintain database build, data cleaning, and data review processes.
- Lead database strategy (build, validation, lock) across studies.
- Partner cross-functionally with Clinical Operations, Clinical Development, Biostatistics, and Safety to ensure study execution and data quality.
Skills and Knowledge
- EDC experience: Medidata RAVE or Veeva.
- GCP, CDISC/CDASH, ICH guidelines, and FDA regulations.
- Excellent verbal/written communication; strong analytical/problem-solving skills.
Basic Requirements
- Bachelor’s or Master’s in Life Sciences, Computer Science, Mathematics, Health Sciences, or related field.
- 12+ years data management experience in pharma/biotech/CRO.
- Proven team leadership/management.
- Oncology therapeutic area experience.
- Ability to manage CRO relationships and data deliverables.
- Experience using AI-enabled tools to improve productivity.
Preferred Requirements
- Veeva EDC system experience.
- Radiopharmaceutical experience.
Benefits/Compensation (as stated)
- Remote (US): $241,768–$292,966.
- Health coverage (medical/pharmacy/dental/vision), 401(k), disability/life insurance; PTO options and global shutdown per eligibility.
Application Instructions
- Contact details and links are provided in the posting, but no specific application steps are included.
- Lead and oversee data management activities across the clinical portfolio, ensuring high-quality, timely, compliant data deliverables.
- Provide strategic leadership for data management in support of NDA submissions (database lock, submission readiness, inspection preparedness).
- Build, lead, and develop the data management team (hiring, performance management, capability development).
- Serve as primary interface with external partners to align on data standards, processes, and resourcing.
- Oversee vendor strategy/performance (selection, budget, timeline oversight, quality assurance).
- Standardize data management processes; develop and implement SOPs for scalable, inspection-ready operations.
- Establish and maintain database build, data cleaning, and data review processes.
- Lead database strategy (build, validation, lock) across studies.
- Partner cross-functionally with Clinical Operations, Clinical Development, Biostatistics, and Safety to ensure study execution and data quality.
Skills and Knowledge
- EDC experience: Medidata RAVE or Veeva.
- GCP, CDISC/CDASH, ICH guidelines, and FDA regulations.
- Excellent verbal/written communication; strong analytical/problem-solving skills.
Basic Requirements
- Bachelor’s or Master’s in Life Sciences, Computer Science, Mathematics, Health Sciences, or related field.
- 12+ years data management experience in pharma/biotech/CRO.
- Proven team leadership/management.
- Oncology therapeutic area experience.
- Ability to manage CRO relationships and data deliverables.
- Experience using AI-enabled tools to improve productivity.
Preferred Requirements
- Veeva EDC system experience.
- Radiopharmaceutical experience.
Benefits/Compensation (as stated)
- Remote (US): $241,768–$292,966.
- Health coverage (medical/pharmacy/dental/vision), 401(k), disability/life insurance; PTO options and global shutdown per eligibility.
Application Instructions
- Contact details and links are provided in the posting, but no specific application steps are included.