Director, Early Clinical Development (Oncology)

Bristol-Myers Squibb • Madison, WI

411d • $279,000 - $321,000 • Hybrid

About The Position

The Director of Early Clinical Development in Oncology at Bristol-Myers Squibb is responsible for overseeing multiple clinical trials, providing medical accountability, and ensuring the successful execution of Phase I/II studies. This role requires a strong background in clinical research and leadership, as well as the ability to collaborate with cross-functional teams to drive early clinical strategy and development of promising drug candidates.

Requirements

• Advanced degree(s) in relevant field: MD, MD/PhD (or x-US equivalent) with clinical expertise in a therapeutic area.
• 5+ years of relevant experience in discovery, translational and/or clinical research in academic or industry setting.
• Strong leadership skills with proven ability to lead and work effectively in a team environment.
• Ability to communicate and present information clearly in scientific and clinical settings.
• Knowledge of drug development process and components needed to execute an effective clinical plan.

Nice To Haves

• Subspecialty fellowship training in applicable therapeutic area preferred.
• Track record of recognized contributions to the field (e.g., publications, patents, keynote participation in conferences).

Responsibilities

• Serve as an independent Medical Monitor for clinical trials from Phase 1 through Proof-of-Concept.
• Articulate clinical development strategy and analyze clinical trial data to support development.
• Provide oversight and medical accountability for multiple trials across early development clinical lifecycle.
• Manage site interactions in partnership with the Clinical Scientist for medical questions and education.
• Assess key safety-related serious adverse events in partnership with Worldwide Patient Safety.
• Contribute to and be a key member of a high performing Study Delivery Team (SDT).
• Collaborate with Clinical Scientists to provide input into protocols and contribute medical strategic oversight.
• Design and develop clinical studies and research plans in support of asset strategy.
• Liaise with Clinical Scientists and Translational & Discovery Scientists to define dose and schedule, indications, and patient selection.
• Lead the analysis of benefit/risk for clinical development protocols in a matrix team environment.
• Maintain a strong medical/scientific reputation within the disease area and keep up to date with relevant literature.
• Contribute to key Health Authority interactions and advisory board meetings as Early Clinical Development Physician.
• Represent the department in business development due diligence and partner alliance management.

Benefits

• Paid holidays
• Disability insurance
• Health insurance
• Dental insurance
• Tuition reimbursement
• Military leave
• Employee assistance program
• Life insurance

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Industry: Chemical Manufacturing
• Education Level: Master's degree