Medical Director, Clinical Development, Oncology (Prostate and Renal Cancers)

Role Summary

Medical Director, Clinical Development, Oncology (Prostate and Renal Cancers) – leads medical/scientific supervision of clinical trials in solid tumor oncology, with potential focus on prostate or renal cancers.

Responsibilities

• 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.

Qualifications

• Required: MD or MD/PhD with a minimum of 3 to 5 years of relevant research experience.
• Preferred: Oncology clinical fellowship training with translational and/or clinical research experience.

Skills

• Clinical trial design and medical oversight in oncology.
• Literature and data review; cross-functional collaboration; scientific communication.

Education

• MD or MD/PhD required.

Additional Requirements

• Onsite work with a 4-day minimum onsite requirement in Tarrytown, NY or Warren, NJ.