Senior Manager, Clinical Data Management

Location: Uxbridge

Hybrid Working: 50% on site

Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.

You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more:

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.

• 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

• 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.

• 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.

• 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.

• 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.

• 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

• A Bachelor's Degree (advanced degree preferred) and at least 5 years of relevant industry experience
• A strong command of clinical drug development…