Associate Director, Clinical Data Management – Uxbridge Join Bristol Myers Squibb as an Associate Director of Clinical Data Management in our Uxbridge site, leading end‑to‑end data management for complex, high‑stakes clinical development programmes. Responsibilities * Own end‑to‑end data management across one or more complex, high‑stakes clinical development programmes, with autonomy to shape how they run. * Set programme‑level data standards in partnership with global teams, leaving a legacy that outlasts any single trial. * Lead data quality review meetings, ensuring integrity and completeness of trial data that underpins regulatory submissions worldwide. * Mentor junior Data Management Leads to grow the next generation of talent and enhance your own leadership reputation. * Represent Data Management on cross‑functional and regulatory submission teams, influencing the organization at the executive level. * Manage EDC systems (Medidata RAVE), integrating data from eCOA, External Data, and Safety Gateway platforms; oversee third‑party vendors and CROs to meet SLAs. * Author and review critical study documentation—Data Quality Management Plans, eCRF Completion Guidelines—and lead or support health authority inspections and audits. * Drive continuous improvement: evaluate new technologies, contribute to functional SOPs, and support change‑management initiatives with broad impact. Qualifications * 7+ years of experience in biopharma or CRO environments, with at least 3 years in a study or programme leadership role. * Strong working knowledge of FDA/ICH guidelines and industry data management practices. * Hands‑on experience with EDC systems, ideally Medidata RAVE. * A sharp eye for metrics, reporting, and quality oversight. * Excellent communication skills; able to hold a room with junior team members and senior regulatory authorities. * Bachelor's degree in life sciences, data science, or statistics (advanced degree is a bonus, not a barrier). Benefits & Logistics * 5–10% travel to industry conferences, investigator meetings, and regulatory inspections. * Hybrid work model possible (Hybrid statement ID: #LI-Hybrid). * Comprehensive benefits package and opportunities for career growth. Equal Employment Opportunity Statement BristolMyersSquibb is an equal‑opportunity employer. We are committed to ensuring that people with disabilities can excel through a transparent recruitment process and reasonable workplace accommodations. We consider qualified applicants with arrest and conviction records as permitted by applicable laws. #J-18808-Ljbffr
