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. Take your career farther than you thought possible.
Position Summary
The Director, Global Clinical Physician is a key member of the Late Clinical Development organization within Hematology, Oncology, and Cell Therapy (HOCT). This role provides medical and scientific leadership for global clinical development programs and contributes to the design, execution, and interpretation of clinical trials from early/late development through registration.
The Director serves as a critical medical expert within cross-functional teams and plays an important role in shaping clinical development strategies to deliver innovative therapies to patients.
Key Responsibilities
Direct Reports: Individual Contributor (no direct reports); matrix leadership responsibilities.
Management Scope: Provides medical leadership across study teams and contributes to Clinical Development Team (CDT).
1. Contribute to global clinical development strategies aligned with asset and disease area priorities
2. Support design and execution of clinical development plans (Phase 1–3)
3. Provide medical input into protocols, endpoints, eligibility criteria, and safety strategy
4. Perform medical monitoring and data review, including safety signal assessment
5. Partner with Clinical Scientists and cross-functional teams to ensure high-quality trial execution
6. Support investigator engagement, site interactions, and medical education activities
7. Contribute to benefit-risk assessment and interpretation of clinical data
8. Maintain awareness of evolving science, treatment landscapes, and competitive environment
9. Support regulatory submissions and interactions with global health authorities
Key requirements
Basic Qualifications
10. MD (or equivalent) required
11. Clinical experience in hematology, oncology, or related therapeutic area
12. Experience in clinical research and drug development
13. Knowledge of GCP, regulatory requirements, and clinical trial processes
14. Strong collaboration skills and ability to work in a matrix environment
Preferred Qualifications
15. Fellowship training in hematology/oncology
16. Experience in late-stage (Phase 2/3 or registrational) clinical development
17. Prior medical monitoring experience
18. Experience interacting with regulatory authorities (FDA, EMA, etc.)
19. Established scientific track record (publications or presentations)
Competencies
20. Strong scientific and clinical judgment
21. Strategic thinking and problem-solving
22. Effective cross-functional collaboration
23. Communication and stakeholder engagement
24. Ability to manage complexity and prioritize across multiple programs
Travel Requirements
Up to ~20–30% domestic and international travel, including investigator meetings and scientific conferences.