Global Director Medical Affairs (gdma) – Precision Medicine Excellence & Operations Lead

Merck Merck · Pharma · NJ

The Global Director Medical Affairs (GDMA) – Precision Medicine Excellence & Operations Lead at Merck is responsible for designing, operationalizing, and improving systems and standards for diagnostic readiness at scale. This role leads the Precision Medicine / Diagnostics Capabilities Program and the Center of Excellence & Innovation Hub, drives global pathology education and medical societies strategy, and ensures operational excellence in cross-asset congress operations and pan-tumor publications. The role requires experience in capability design, implementation, and program management within a global matrix environment, with a focus on precision medicine and diagnostics in the pharmaceutical/biotech industry.

What you'd actually do

  1. Design, implement, and continuously evolve the Precision Medicine / Diagnostics Capabilities Program, ensuring alignment with portfolio priorities and launch timelines.
  2. Own the capability maturity framework (e.g. IRSAT [Implementation Readiness Self-assessment Tool] or equivalent), providing global readiness intelligence, gap identification, and prioritization of capability investments.
  3. Lead the Precision Medicine Center of Excellence & Innovation Hub, ensuring it functions as a one‑stop hub for: knowledge capture and reuse, best‑practice identification and dissemination, and codification of lessons learned into standards and operating models.
  4. Design and lead a global pathology education strategy that supports diagnostic capability maturation across priority tumors and indications.
  5. Coordinate cross‑asset congress operations for Precision Medicine‑relevant activities (e.g., playbooks, our research division's debriefs, SL engagements), ensuring operational consistency, efficiency, and alignment with Precision Medicine capability and readiness goals.

Skills

Required

  • Advanced life sciences degree preferred (M.D., PhD, PharmD, or MSc., with significant scientific/technical experience); equivalent demonstrated scientific and diagnostics credibility accepted.
  • Minimum 3 years’ experience in pharmaceutical/biotech industry with substantive Medical Affairs experience and a strong focus on precision medicine, diagnostics, or related capabilities (e.g., biomarker operations, diagnostic partnerships, pathology education).
  • Demonstrated experience in capability design and implementation (e.g., frameworks, training programs, maturity models) and/or Center of Excellence / excellence program leadership.
  • Proven track record working in global matrix environments, collaborating across Medical Affairs, Market Access, Regulatory, Clinical Development, and Operations.
  • Strong experience in program and operations management, including coordination of complex cross‑asset initiatives such as congress operations and publication planning.
  • Excellent communication, facilitation, and change‑management skills; ability to translate complex information into clear, actionable guidance.

What the JD emphasized

  • Minimum 3 years’ experience in pharmaceutical/biotech industry with substantive Medical Affairs experience and a strong focus on precision medicine, diagnostics, or related capabilities
  • Demonstrated experience in capability design and implementation (e.g., frameworks, training programs, maturity models) and/or Center of Excellence / excellence program leadership
  • Proven track record working in global matrix environments
  • Strong experience in program and operations management