Senior Manager, Clinical Data Management Uxbridge - GB R Posted 10 hours ago

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Working with Us

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.

Bristol Myers Squibb recognises 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.

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.

What You'll Be Doing

• Leading end-to-end clinical data management for complex and impactful trials.
• Driving data collection strategy across one or more complex clinical development projects, aligning cross-functional teams around clear, high-quality standards.
• Owning the full data management lifecycle, from planning and collection through to clean, submission-ready datasets delivered on time.
• Shaping the systems that power our trials, leading requirements gathering for EDC platforms and collaborating with partners across eCOA, External Data, and Safety Gateway.
• Chairing Data Quality Review meetings to keep trial data current, complete, and audit-ready at every stage.
• Authoring and reviewing key study documents, ensuring consistency and compliance across the board.
• Coaching and guiding junior Data Management Leads, helping them grow while raising the overall capability of the team.
• Representing DM at cross-functional project teams and regulatory submission teams, being a key player during Health Authority inspections and audits.
• Monitoring deliverables, managing data currency throughout the trial, and holding partners accountable to SLAs.
• Contributing 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).
• Intellectual challenge, work with cutting-edge data collection technologies and emerging industry trends.

What You'll Bring

• A Bachelor's Degree (advanced degree preferred) and at least 5 years of relevant industry experience.
• A strong command of clinical drug development processes, FDA/ICH guidelines, and data management best practices.
• Hands-on experience with EDC systems; Medidata RAVE experience is a strong plus.
• Proven project management skills, with a PMP certification considered a bonus.
• The ability to translate complex data into clear insights through metrics analysis and reporting.
• Outstanding communication skills, whether presenting to senior leadership or collaborating with a vendor team.
• Familiarity with submission requirements including NDA, BLA, and MAA processes.

Ready to Apply? If you're someone who takes pride in doing rigorous work and inspiring others to do the same, we'd love to hear from you. Join BMS. Transform patients' lives. Build your own.

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as "Transforming patients' lives through scienceTM", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles.

Data Protection: We will never request payments, financial information, or social security numbers during our application or recruitment process.