Senior Medical Director, Oncology Clinical Development (Solid Tumors)
$211,000–$400,500 year
HybridWaltham, Massachusetts, United States
Job Summary
Manage the design, implementation, and oversight of one or more clinical development programs in solid tumors, ensuring adherence to Good Clinical Practices, regulatory requirements, and safety standards. Oversee study enrollment, timelines, and the interpretation of accumulating data on safety and efficacy while coordinating with Clinical Operations and cross-functional teams. Direct Medical Directors and Clinical Scientists, chair the Clinical Strategy Team to develop vetted development plans, and serve as the clinical interface for opinion leader interactions and regulatory discussions. Contribute to translational strategies and business development activities as needed. Requires an M.D. or D.O. degree with relevant therapeutic specialty, two years of clinical trial experience, and the ability to lead moderate-complexity research programs globally.
Required Qualifications
- Medical Doctor (M.D.)
- Doctor of Osteopathy (D.O.)
- non-US equivalent of M.D. degree
- relevant therapeutic specialty in an academic or hospital environment
- Completion of a residency program
- At least 2 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent
- Ability to run a clinical research program of moderate complexity with minimal supervision
- Ability to perform and bring out the best in others on a cross-functional global team
- Ability to interact externally and internally to support a global scientific and business strategy
- Knowledge of clinical trial methodology
- Knowledge of regulatory and compliance requirements governing clinical trials
- Experience in development of clinical strategy
- Experience in the design of study protocols
- Excellent oral and written English communication skills
Desired Qualifications
- Completion of a subspecialty fellowship
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