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      Role Summary
 Medical Director, Clinical Development, Oncology (Gynecologic Cancers) - A physician-scientist with exceptional academic clinical trials experience, preferably in solid tumor oncology drug development. Responsible for medical/scientific supervision of clinical trials and for drafting study concepts leading to clinical trial protocols. May work on studies in gynecologic cancers.
 
 Responsibilities
 
 - Defines clinical trial-related goals and objectives.
 
 - Conducts literature and database research on clinical trials as needed.
 
 - Collaborates with Clinical Project Managers and Clinical Trial Managers at the study level and with the Therapeutic Area Program Manager.
 
 - Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings.
 
 - Leads and supervises the Clinical Team to produce high quality program deliverables on schedule.
 
 - Maintains and develops relationship with key study investigators.
 
 
 
 Qualifications
 
 - Required: MD or MD/PhD with a minimum of 3 to 5 years of relevant research experience.
 
 - Preferred: Oncology clinical fellowship training with translational and/or clinical research experience.
 
 
 
 Skills
 
 - Clinical trial design and protocol development
 
 - Medical/scientific supervision of clinical trials
 
 - Literature and data analysis related to oncology clinical research
 
 - Collaboration across cross-functional teams
 
 
 
 Education
 
 
 Additional Requirements
 
 - 4-day onsite minimum requirement in Tarrytown, NY or Warren, NJ.