Director, MEG Lead Oncology, Medical Evidence Generation

Role Summary

The Medical Evidence Generation (MEG) Lead in Oncology oversees evidence generation for the Oncology portfolio, including CRCs, MAST, and ISRs, to accelerate pipeline development. Responsible for fostering relationships with thought leaders, managing study lifecycles, and addressing evidence gaps through external partnerships.

Responsibilities

• Facilitate collaborative exchange between BMS and thought leaders in community practice and academia, representing BMS as a trusted, inclusive, and innovative partner.
• Deliver CRCs, ISRs, and MASTs from concept ideation to governance approval and throughout the study lifecycle.
• Serve as the point of contact for CRCs, ISRs, and MASTs within Therapeutic and Disease area teams.
• Design and drive strategies to accelerate development of the clinical development pipeline leveraging external research platforms, technologies, and insights.
• Advise senior functional and therapeutic area leaders on external opportunities to inform strategy and integrated evidence generation plans.
• Lead a limited number of high-visibility projects leveraging disease subject matter expertise.
• Contribute to the evolution of MEG therapeutic area strategy and value proposition.
• This position is based at Lawrenceville (PPK), Madison (GIR), New Jersey or Boudry (Switzerland).

Qualifications

• Advanced scientific degree (MD, PhD, or PharmD or equivalent) with extensive scientific/clinical experience.
• At least 7 years of experience in pharmaceutical clinical development, Medical Affairs, or relevant Commercial experience; customer-facing experience is desirable.
• Ability to strategically analyze data generation opportunities with minimal supervision.
• Ability to develop and sustain high-performing relationships with external thought leaders and internal stakeholders.
• Strong leadership, credibility with external investigators, and the ability to balance business and scientific acumen.
• Understanding of global healthcare systems and academic settings; ability to lead in ambiguous environments.
• Exceptional communication and interpersonal skills to influence decisions at all levels.
• Strong knowledge of project planning and management of clinical trials.
• Ability to partner across functions and levels within the enterprise.
• Travel: Expected 30% travel globally.

Skills

• Strategic thinking and opportunity assessment
• Relationship-building with external thought leaders
• Cross-functional collaboration and influence
• Clinical trial design and lifecycle management
• Effective communication and negotiation

Education

• Advanced degree required: MD, PhD, PharmD or equivalent.

Additional Requirements

• Travel up to 30% globally.