Senior Manager, Clinical Data Management (R1601559)
As our Senior Manager of Clinical Data Management, you will lead end‑to‑end clinical data management for complex and high‑impact trials. You will be the go‑to person for internal teams and external partners, set the bar for data quality, and help shape the speed and quality of medicines reaching patients worldwide.
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
- Monitor deliverables, manage data currency throughout the trial, and hold partners accountable to SLAs that protect the integrity of our work
Driving Continuous Improvement
- Contribute to organizational evolution by 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 worldwide
- Career elevation: 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 that keep your skills sharp and future‑proof
What You’ll Bring
- Bachelor’s Degree (advanced degree preferred) and at least five years of relevant industry experience
- 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; PMP certification considered a bonus
- Ability to translate complex data into clear insights through metrics analysis and reporting
- Outstanding communication skills, able to present to senior leadership and collaborate with vendor teams
- Familiarity with submission requirements including NDA, BLA, and MAA processes
Equal Employment Opportunity
Bristol Myers Squibb is an equal opportunity employer. We are committed to ensuring people with disabilities can excel through a transparent recruitment process and reasonable workplace accommodations.
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. All data processed in connection with role applications is treated in accordance with applicable data privacy policies and regulations.
Candidate Rights
BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
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