At a Glance
- Tasks: Lead global clinical development for innovative therapies in hematology and oncology.
- Company: Join a leading biopharmaceutical company committed to diversity and innovation.
- Benefits: Competitive salary, comprehensive health benefits, and opportunities for professional growth.
- Other info: Dynamic role with travel opportunities and a focus on collaboration.
- Why this job: Make a real impact on patient lives through cutting-edge clinical research.
- Qualifications: MD required with clinical experience in hematology or oncology.
The predicted salary is between 80000 - 100000 £ per year.
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
- Contribute to global clinical development strategies aligned with asset and disease area priorities.
- Support design and execution of clinical development plans (Phase 1–3).
- Provide medical input into protocols, endpoints, eligibility criteria, and safety strategy.
- Perform medical monitoring and data review, including safety signal assessment.
- Partner with Clinical Scientists and cross‑functional teams to ensure high‑quality trial execution.
- Support investigator engagement, site interactions, and medical education activities.
- Contribute to benefit‑risk assessment and interpretation of clinical data.
- Maintain awareness of evolving science, treatment landscapes, and competitive environment.
- Support regulatory submissions and interactions with global health authorities.
Key Requirements
- MD (or equivalent) required.
- Clinical experience in hematology, oncology, or related therapeutic area.
- Experience in clinical research and drug development.
- Knowledge of GCP, regulatory requirements, and clinical trial processes.
- Strong collaboration skills and ability to work in a matrix environment.
Preferred Qualifications
- Fellowship training in hematology/oncology.
- Experience in late‑stage (Phase 2/3 or registrational) clinical development.
- Prior medical monitoring experience.
- Experience interacting with regulatory authorities (FDA, EMA, etc.).
- Established scientific track record (publications or presentations).
Competencies
- Strong scientific and clinical judgment.
- Strategic thinking and problem‑solving.
- Effective cross‑functional collaboration.
- Communication and stakeholder engagement.
- 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.
Equal Opportunity Employer Statement
Bristol Myers Squibb is an equal opportunity employer and welcomes diversity. All qualified individuals are encouraged to apply.
Director, Global Clinical Physician, Late HOCT employer: Bristol Myers Squibb
Bristol Myers Squibb is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration in the field of hematology, oncology, and cell therapy. With a strong commitment to employee growth, we provide ample opportunities for professional development and engagement in groundbreaking clinical research, all while being part of a diverse and inclusive team dedicated to delivering transformative therapies to patients worldwide.
