Senior Medical Director leading clinical trial development and oversight at Pfizer. Focusing on GU oncology with responsibilities including medical monitoring and strategic guidance.
About the role
- Executive/Senior Medical Director providing medical leadership for oncology drug development at Verastem. Managing clinical studies and ensuring compliance in a hybrid work environment.
Responsibilities
- Provide medical and scientific leadership for Verastem’s KRAS G12D ON/OFF inhibitor: VS-7375 Program
- Serve as the Clinical Lead for one or more studies
- Support the design and execution of assigned clinical trial(s)
- Ensure compliance and patient safety as the primary medical/safety contact
- Collaborate with Clinical Science, Data Management, and Statistical Programming
- Lead regular data reviews to guide development strategy
- Author key study and regulatory documents
- Contribute to scientific publications
- Represent the study/program and interact with key internal/external partners
- Maintain scientific and clinical knowledge in oncology and provide input on pipeline
Requirements
- Medical Degree (M.D. or equivalent) required
- 5 + years of experience in biotech / pharma industry oncology drug development
- Knowledge of Good Clinical Practices (cGCP)
- Comprehensive knowledge of clinical trial design
- Understanding of the overall global drug development process
- Knowledge of current external regulatory environment, e.g. FDA, EMA requirements
- Excellent interpersonal, verbal communication, and influencing skills
- Strong analytical and presentation skills
- Ability to travel up to 20% of the time
Benefits
- Health insurance
- Retirement plans
- Paid time off
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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