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About the Role
As Director, Global Clinical Trial Physician, you will be a core contributor to the Global Clinical Development Strategy for your assigned asset and indication, actively shaping the strategy rather than executing someone else's vision. You will bring scientific depth, regulatory knowledge, and cross-functional credibility to ensure clinical studies are designed, conducted, and reported effectively, ultimately accelerating the delivery of innovative medicines to patients.
Responsibilities
- Serve as the subject matter expert for the development, conduct, and regulatory submission of clinical studies across your portfolio, from protocol development through CSR review and validation.
- Contribute meaningfully to clinical development plans, strategic discussions, and the harmonization of standards across programs and indications.
- Lead clinical oversight of study data, guiding teams in understanding CRF interdependencies, data conventions, review tools, and visualizations in collaboration with Data Management and Programming.
- May serve as Trial Lead for complex clinical studies, taking the helm on work that demands experience, judgment, and the ability to hold a team together under pressure.
- Present data and insights to internal and external stakeholders, including investigators, study staff, and senior leadership, with credibility and strong communication skills.
- Partner with the CCOE Clinical Capabilities Team to lead and support process improvements and departmental training, sharing best practices, communicating lessons learned, and serving as a peer coach and mentor.
Requirements
- Degree in Life Sciences - MD, PhD, PharmD, MS, RN or equivalent scientific discipline
- 10+ years of experience in Clinical R&D, including operating in a matrix environment
- Recognized expertise in your Therapeutic Area and/or Clinical Science function
- Advanced knowledge of GCP/ICH guidelines and the full drug development lifecycle - from discovery through to registration
- Strong understanding of study design, statistics, clinical operations, and the regulatory environment
- Experience with protocol development, data review, CSR validation, and regulatory documentation
Skills
- Scientific depth in therapeutic area
- Advanced skills in scientific data review, trend identification, interpretation, and reporting
- Influential communication of complex scientific information
- Cross-functional relationship building
- Proactive and results-driven approach
- Commitment to high scientific and regulatory standards
- Adaptability under pressure
- Coaching and mentoring abilities
Location
- Hybrid
Work Type
- Hybrid
Experience Level
- Director level
- 10+ years of experience
Education Level
- MD, PhD, PharmD, MS, RN or equivalent scientific discipline
Benefits
- Opportunities for growth
- Supportive environment
- Inclusion
- Wellbeing
- Flexibility
- Comprehensive benefits
About the Company
- Bristol Myers Squibb is one of the most innovative biopharmaceutical companies on the planet, with a pipeline and a portfolio that offers genuinely fascinating, career-defining work.
- Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
- We are dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles.
- Bristol Myers Squibb is Disability Confident – Employer.
Equal Opportunity
- We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.
- BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
- We will never request payments, financial information, or social security numbers during our application or recruitment process.
- Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.