Executive / Senior Medical Director, Clinical Development

Responsibilities

• Supports the design and execution of assigned clinical trial(s) and works closely with cross functional study team members to execute activities associated with the conduct of the clinical trials. - Serves as the primary medical / safety contact for assigned clinical trials, ensuring compliance and patient safety. Serve as the primary contact for medical-related inquiries from investigators, regulatory agencies, and internal/external teams, ensuring consistent protocol interpretation and clarification. - Partners with Clinical Science, Data Management, Statistical Programing to ensure data integrity. Lead regular data reviews and insight generation to guide development strategy. - Collaborates with Safety on reporting of identified adverse events (AEs), serious adverse events (SAEs), and other safety-related events. Contributes to safety profile characterization and corresponding risk mitigation strategy / plans. - Acts as a key member of the Program Team to devise integrated development plan(s) and development / regulatory strategies. - Authors and develop key study and regulatory documents with the cross functional team, including, but not limited to study protocol, investigator brochure, informed consent form, and clinical study reports. Contributes to scientific publications, including conference abstracts and peer-reviewed journal articles. - Represents the study / program and interacts on a regular basis with key internal / external partners and stakeholders, including key opinion leaders, clinical investigators, clinicians, scientists as well as internal leadership team and R&D. Lead and present at investigator meetings and advisory committees. - Maintains scientific and clinical knowledge in oncology and provides input on Verastem’s pipeline, translational and preclinical work. Required qualifications