Medical Director, Oncology Clinical Development - GU
GSK
August 29, 2026
Remote friendly (Waltham, MA)
United States
Clinical Research and Development
Medical Director, Oncology Clinical Development – GU (Genitourinary)
In This Role You Will:
- Serve as physician in the clinical program team for study design, conduct, safety oversight, and data interpretation
- Lead medical monitoring to ensure patient safety, clinical integrity, and compliance with protocol and regulations
- Interpret clinical and safety data to inform study/program decisions led by the CDL
- Partner with the Senior Scientist and cross-functional teams to integrate medical input into execution
- Provide medical input to protocol development and key study documents (e.g., ICF, PDMP, SRM)
- Serve as a core member of the Clinical Matrix Team (CMT); engage investigators/KEEs; represent medical perspective in regulatory and external interactions
Detailed Responsibilities:
- Lead medical monitoring/real-time eligibility and safety oversight; review trial data (including delegated review)
- Interpret safety signals with pharmacovigilance; participate in SRT/IDMC/internal safety forums; ensure GCP/ICH compliance
- Contribute to scientific communications and investigator collaboration on abstracts/posters/manuscripts
Why You? (Qualifications)
- MD (or equivalent) with board certification/eligibility in oncology/haematology/related specialty
- Oncology clinical experience with exposure to clinical research/drug development
- Demonstrated clinical trial conduct experience (medical monitoring, safety review, data interpretation)
- Knowledge of GCP, ICH, and global regulatory frameworks; strong clinical judgement and scientific communication
Preferred:
- Phase I–III oncology GU experience; regulatory interaction experience; engagement with KEEs/investigators; clinical publications/congress; oncology disease biology expertise; medical monitoring across multiple studies/programs
Working model:
- Hybrid; on-site at posted locations at least 2 days/week.
Compensation/Benefits (if applicable in posting):
- US base salary (Cambridge, MA; Waltham, MA; Rockville, MD; San Francisco, CA): $189,750–$316,250; annual bonus; eligibility for share-based long-term incentive; health insurance, retirement, paid holidays/vacation, paid caregiver/parental and medical leave.
In This Role You Will:
- Serve as physician in the clinical program team for study design, conduct, safety oversight, and data interpretation
- Lead medical monitoring to ensure patient safety, clinical integrity, and compliance with protocol and regulations
- Interpret clinical and safety data to inform study/program decisions led by the CDL
- Partner with the Senior Scientist and cross-functional teams to integrate medical input into execution
- Provide medical input to protocol development and key study documents (e.g., ICF, PDMP, SRM)
- Serve as a core member of the Clinical Matrix Team (CMT); engage investigators/KEEs; represent medical perspective in regulatory and external interactions
Detailed Responsibilities:
- Lead medical monitoring/real-time eligibility and safety oversight; review trial data (including delegated review)
- Interpret safety signals with pharmacovigilance; participate in SRT/IDMC/internal safety forums; ensure GCP/ICH compliance
- Contribute to scientific communications and investigator collaboration on abstracts/posters/manuscripts
Why You? (Qualifications)
- MD (or equivalent) with board certification/eligibility in oncology/haematology/related specialty
- Oncology clinical experience with exposure to clinical research/drug development
- Demonstrated clinical trial conduct experience (medical monitoring, safety review, data interpretation)
- Knowledge of GCP, ICH, and global regulatory frameworks; strong clinical judgement and scientific communication
Preferred:
- Phase I–III oncology GU experience; regulatory interaction experience; engagement with KEEs/investigators; clinical publications/congress; oncology disease biology expertise; medical monitoring across multiple studies/programs
Working model:
- Hybrid; on-site at posted locations at least 2 days/week.
Compensation/Benefits (if applicable in posting):
- US base salary (Cambridge, MA; Waltham, MA; Rockville, MD; San Francisco, CA): $189,750–$316,250; annual bonus; eligibility for share-based long-term incentive; health insurance, retirement, paid holidays/vacation, paid caregiver/parental and medical leave.