Medical Director, Clinical Development, Oncology

Role Overview:
- Qualified physician scientist with exceptional academic clinical trials experience, preferably in solid tumor oncology drug development.
- Drafts designs for clinical study concepts leading to clinical trial protocols.
- Provides medical/scientific supervision of individual clinical trials (melanoma, lung, breast, gastric, or colorectal cancers).

As a Medical Director, a typical day includes:
- 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 relationships with key study investigators.

This Role May Be For You If:
- You are passionate about impacting entire populations of patients.
- You want to learn innovative approaches to drug development.
- You want to be part of a collaborative, growing team.

To be considered:
- MD or MD/PhD with 3 to 5 years of relevant research experience.
- Oncology clinical fellowship training with translational and/or clinical research experience (strongly preferred).

Location/Onsite:
- 4-day onsite minimum requirement in Tarrytown, NY or Warren, NJ.

Application instructions:
- Apply now.