Senior Manager, Clinical Data Management

Senior Manager, Clinical Data Management (R1603294)

Senior Manager, Clinical Data Management

What You’ll Be Doing

Leading Where It Matters Most

• 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

• Coach and guide junior Data Management Leads, helping them grow while raising the overall capability of the team

Representing DM at the Highest Level

• Participate in cross‑functional project teams and regulatory submission teams, and serve as a key player during Health Authority inspections and audits

Vendor Oversight & Partnerships

• Work with FSPs, CROs, and third‑party vendors, monitoring deliverables, managing data currency throughout the trial, and holding partners accountable to SLAs that protect the integrity of our work

Driving Continuous Improvement

• Contribute to CAPA implementation and bring 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: attend 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 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, you know how to land the message
• Familiarity with submission requirements including NDA, BLA, and MAA processes

Equal Employment Opportunity Statement

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Bristol Myers Squibb is Disability Confident – Employer.

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