Senior Manager, Clinical Data Management

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. Location: Uxbridge Hybrid Working: 50% on site Are you ready to do the work of your career? At Bristol Myers Squibb, we believe that the right data, in the right hands, at the right time can change everything. Every clinical trial we run brings us closer to a treatment that could transform or save a patient's life. As our Senior Manager of Clinical Data Management,  you'll be the person who makes that possible. This isn't just a data role. It's a leadership position at the heart of our R&D pipeline; where your decisions, your standards, and your expertise directly shape the speed and quality of life-changing medicines reaching patients worldwide.

Leading Where It Matters Most You'll take the wheel on end-to-end clinical data management for some of our most complex and impactful trials. That means being the go-to person for both internal teams and external partners, the one who sets the bar for data quality and makes sure everyone clears it. Drive data collection strategy across one or more complex clinical development projects, aligning cross-functional teams around clear, high-quality standards Own the full data management lifecycle, from planning and collection through to clean, submission-ready datasets delivered on time Shape the systems that power our trials, leading requirements gathering for EDC platforms and collaborating with partners across eCOA, External Data, and Safety Gateway Chair Data Quality Review meetings to keep trial data current, complete, and audit-ready at every stage Author and review key study documents, Data Quality Management Plans, Data Validation Plans, eCRF Completion Guidelines and more, ensuring consistency and compliance across the board Mentoring the Next Generation One of the most rewarding parts of this role? You'll coach and guide junior Data Management Leads, helping them grow while raising the overall capability of the team. Your expertise becomes their foundation. Representing DM at the Highest Level You'll sit at the table for cross-functional project teams and regulatory submission teams, and you'll be a key player during Health Authority inspections and audits. This is a role where your voice carries real weight. Vendor Oversight & Partnerships Whether working with FSPs, CROs, or third-party vendors, you'll be the quality compass; monitoring deliverables, managing data currency throughout the trial, and holding partners accountable to SLAs that protect the integrity of our work. Driving Continuous Improvement You'll contribute meaningfully to how we evolve as an organisation — supporting CAPA implementation and bringing fresh thinking to continuous improvement initiatives within Clinical Data Management. What's In It For You Meaningful impact , your work directly supports the development of medicines that matter to millions of patients globally Career elevation , step into a senior leadership role with visibility across R&D and a clear path toward Director-level progression Cross-functional influence,  build relationships across clinical operations, regulatory, biostatistics, and beyond Industry exposure , travel to conferences, investigator meetings, and regulatory engagements (approximately 5–10% travel) to stay at the forefront of your field Intellectual challenge , work with cutting-edge data collection technologies and emerging industry trends that keep your skills sharp and future-proof What You'll