Salary
💰 $280,700 - $379,900 per year
About the role
- Drafts and designs clinical study concepts leading to clinical trial protocols
- Responsible for medical/scientific supervision of individual clinical trials
- May work on melanoma, lung, breast, gastric, or colorectal cancer studies
- Defines clinical trial-related goals and objectives
- Conducts literature and database research on clinical trials
- Collaborates with Clinical Project Managers, Clinical Trial Managers, and 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 3 to 5 years of relevant research experience
- Oncology clinical fellowship training with translational and/or clinical research experience strongly preferred
- Exceptional academic clinical trials' experience, preferably in solid tumor Oncology drug development
- Experience drafting designs of clinical study concepts and clinical trial protocols
- Ability to provide medical/scientific supervision of individual clinical trials
- Experience collaborating with Clinical Project Managers, Clinical Trial Managers, and Therapeutic Area Program Managers
- Willingness to be onsite minimum 4 days per week in Tarrytown, NY or Warren, NJ