Assoc. Dir, Medical Affairs

Merck & Co., Inc.

Hybrid
Country medical affairs plan execution
Scientific engagement with key decision makers
Cross-functional collaboration with marketing and regulatory
The Associate Director of Medical Affairs at Merck & Co., Inc. is responsible for leading the execution of the Country Medical Affairs Plan, focusing on vaccines and infectious diseases. This role involves cross-functional collaboration, scientific engagement, and ensuring the delivery of reliable scientific information to enhance patient outcomes

Job Summary

  • The Associate Director is responsible for developing and executing the Country Medical Affairs Plan while spending 20%-30% of time on scientific engagements.
  • This role requires close collaboration with cross-functional teams including Marketing, Market Access, and Regulatory Affairs to align global strategies with local needs.
  • The position involves leading non-promotional medical educational programs and providing balanced scientific information in compliance with company standards and local regulations.

Matching Summary

Match Score: 85

The Associate Director of Medical Affairs at Merck & Co., Inc. is responsible for leading the execution of the Country Medical Affairs Plan, focusing on vaccines and infectious diseases. This role involves cross-functional collaboration, scientific engagement, and ensuring the delivery of reliable scientific information to enhance patient outcomes.

Skills & Requirements

Must-have

  • Country Medical Affairs Plan execution
  • Scientific engagement with key decision makers
  • Cross-functional collaboration with Marketing and Regulatory
  • Budget management for medical education programs
  • Non-promotional scientific information provision

Nice-to-have

  • Building trust with external scientific community
  • Adaptability to local corporate needs
  • Experience with Investigator-Initiated Studies
  • Peer-to-peer medical exchange facilitation

Key Requirements

  • Medical Knowledge in Vaccines and Infectious Disease
  • Clinical Development and Clinical Trials experience
  • Budget Management capabilities
  • Strategic Planning skills
  • Regulatory Training knowledge

Work Rights

Not specified

Tailored Resume

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