Salary
💰 $280,700 - $379,900 per year
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