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
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