Regional Medical Scientific Director (Gynecologic Oncology)

Merck

Madison (WI)

Remote

USD 210,000 - 331,000

Full time

7 days ago
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Job summary

Merck seeks a Regional Medical Scientific Director to serve as a therapeutic and disease expert, engaging in scientific exchanges with Scientific Leaders and providing balanced, non-product information. The role spans scientific exchange, research, congress support, and insights.

The position covers IN, KY, WV, and VA with up to 50% travel. Requires doctoral degree and at least 3 years of relevant experience, plus strong stakeholder management and knowledge of FDA and GCP guidelines.

Qualifications

  • PhD, PharmD, DNP, DO, or MD required.
  • Minimum 3 years of relevant therapeutic area experience beyond degree program.
  • Ability to conduct doctoral-level discussions with external stakeholders.
  • Commitment to scientific excellence and education.

Responsibilities

  • Develops professional relationships with national and regional SLs to ensure access to approved medical and scientific information.
  • Conducts peer-to-peer scientific discussions and maintains a reliable presence with SLs.
  • Addresses scientific questions and directs SL inquiries to appropriate resources.
  • Maintains current knowledge of AOI for the therapeutic area.

Skills

Gynecologic Oncology
Medical Affairs
Medical Knowledge
Oncology
Pharmaceutical Medical Affairs
Professional Networking
Scientific Communications
Scientific Research
Stakeholder Engagement

Education

PhD
PharmD
DNP
DO
MD

Tools

Microsoft Office Suite
Virtual meeting platforms

Job description

Merck seeks a Regional Medical Scientific Director to serve as a therapeutic and disease expert, engaging in scientific exchanges with Scientific Leaders and providing balanced, non-product information. The role spans scientific exchange, research, congress support, and insights.

The position covers IN, KY, WV, and VA with up to 50% travel. Requires doctoral degree and at least 3 years of relevant experience, plus strong stakeholder management and knowledge of FDA and GCP guidelines.

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