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Hybrid Medical Director, Clinical Development – Oncology, Prostate and Renal Cancers
Posted last month
About the role
- Drafts designs of clinical study concepts leading to clinical trial protocols
- Medical/scientific supervision of individual clinical trials
- Defines clinical trial-related goals and objectives
- Conducts literature and database research on clinical trials
- 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
- May work on studies in prostate or renal cancers
Requirements
- MD or MD/PhD
- 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
- Willingness to be onsite a minimum of 4 days per week in Tarrytown, NY or Warren, NJ
- Willingness to undergo background checks as required by law
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
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