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Director, Global Medical Evidence Generation Lead, Oncology

Job in Camden, Camden County, New Jersey, 08100, USA
Listing for: Bristol-Myers Squibb
Full Time position
Listed on 2026-06-19
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 207490 - 251433 USD Yearly USD 207490.00 251433.00 YEAR
Job Description & How to Apply Below

Director of Medical Evidence Generation – Oncology

Position Summary:

The Director of Medical Evidence Generation in Medical Affairs will lead the strategic development and execution of a robust evidence generation plan for a key asset within the Oncology portfolio, focused primarily in gastrointestinal (GI) and genitourinary (GU) cancers. The role includes clinical research collaborations (CRCs), medical affairs sponsored trials (MAST), and investigator-sponsored research studies (ISRs) to uncover new clinical development opportunities and address unmet needs.

Responsibilities
  • Define and drive the integrated evidence generation strategy aligned with Medical Affairs and overall product strategy, spanning clinical trials (Phase II/IV), real‑world evidence, non‑interventional studies, registries, observational research, and health outcomes studies.
  • Critically assess the design of research concepts to ensure strategic alignment with BMS priorities and ability to achieve objectives.
  • Lead or significantly contribute to protocol development, including study design, objectives and endpoints, eligibility criteria, statistical considerations (in collaboration with Biostatistics), and operational feasibility.
  • Engage in peer‑to‑peer scientific dialogue with external research partners to optimize study design.
  • Be accountable for delivering studies from concept ideation to governance approval and throughout the study lifecycle.
  • Serve as a thought leader on evidence generation methodologies to ensure plans are fit‑for‑purpose and impactful.
  • Lead preparation and delivery of evidence generation proposals, updates, and results to internal governance bodies and cross‑functional stakeholders.
  • Apply strong understanding of GCP, ICH guidelines, and clinical trial governance to ensure compliant and high‑quality study execution.
  • Partner with Clinical Operations and CROs to ensure studies are delivered on time, on budget, and with high data quality.
  • Participate in advisory boards, steering committees, and scientific forums as necessary.
  • Collaborate with cross‑functional partners to ensure cohesive planning and execution across geographies and therapeutic areas.
  • Oversee operational delivery of studies, ensuring scientific rigor, quality, compliance, timelines, and budgets.
  • Contribute to scientific dissemination through publications, abstracts, congress presentations, and advisory boards.
Qualifications & Experience
  • Advanced scientific degree (MD, PhD, PharmD, MS or equivalent) with extensive, relevant scientific or strong clinical development experience.
  • At least 5 years of experience in pharmaceutical clinical development, Medical Affairs, and/or relevant commercial experience; prior customer‑facing role highly desirable.
  • Deep understanding of clinical research and evidence generation methodologies.
  • Deep oncology therapeutic area expertise, with a focus in GI and GU cancers.
  • Demonstrated ability to strategically analyze data generation opportunities with minimal supervision.
  • Expertise in critically reviewing key study design elements to ensure objectives can be met.
  • Strategic thinker with strong execution discipline.
  • Demonstrated ability to develop and sustain high‑performing, peer relationships with external thought leaders and internal matrix stakeholders.
  • Understanding of global healthcare systems and academic settings with ability to lead in ambiguous and changing environments.
  • Exceptional communication and interpersonal skills to influence decision‑making at all levels.
  • Proven experience leading cross‑functional study teams and governance interactions.
  • Expected 20% travel globally.
Location

This position is based at Lawrenceville (PPK) or Madison (GIR) New Jersey.

Compensation Overview

Madison – Giralda – NJ – US: $207,490 – $251,433
Princeton – NJ – US: $207,490 – $251,433

Benefits
  • Health Coverage:
    Medical, pharmacy, dental, and vision care.
  • Well‑being Support:
    Programs such as BMS Well‑Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
  • Financial Protection: 401(k) plan, short‑term and long‑term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal…
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