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Hybrid Medical Director, Clinical Development, Oncology – Gynecologic Cancers
Posted last month
About the role
- Drafts designs of clinical study concepts which lead to clinical trial protocols
- Responsible for medical/scientific supervision of individual clinical trials
- May work on studies in gynecologic cancers
- Defines clinical trial-related goals and objectives
- Conducts literature and database research on clinical trials as needed
- Collaborates with Clinical Project Managers, Clinical Trial Managers, and 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 relationships with key study investigators
Requirements
- MD or MD/PhD required
- Minimum of 3 to 5 years of relevant research experience
- Qualified physician scientist with exceptional academic clinical trials' experience, preferably in solid tumor Oncology drug development
- Oncology clinical fellowship training with translational and/or clinical research experience strongly preferred
- Experience drafting clinical study concepts and clinical trial protocols
- Ability to provide medical/scientific supervision of individual clinical trials
- 4-day onsite minimum requirement in Tarrytown, NY or Warren, NJ
Benefits
- Comprehensive benefits (depending on location)
- Health and wellness programs
- Fitness centers
- Equity awards
- Annual bonuses
- Paid time off for eligible employees at all levels
- Inclusive and diverse culture
- Reasonable accommodation for known disabilities or chronic illnesses
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