Assoc. Dir, Medical Affairs Respiratory

Merck & Co., Inc.

Not specified; not specified; not specified
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Country medical affairs plan execution
Scientific engagement with key decision makers
Cross-functional collaboration with marketing
** The Associate Director of Medical Affairs at Merck & Co., Inc. is responsible for leading the development and execution of the Country Medical Affairs Plan, collaborating with scientific leaders and cross-functional teams to enhance patient outcomes. The role involves strategic leadership, scientific engagement, and budget management within a hybrid work environment. **

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 cross-functional collaboration with Marketing, Market Access, Regulatory Affairs, and Pharmacovigilance teams to align strategies.
  • The position involves providing non-promotional, balanced scientific information and leading local Group Input Meetings to support optimal patient outcomes.

Matching Summary

Match Score: 75

** The Associate Director of Medical Affairs at Merck & Co., Inc. is responsible for leading the development and execution of the Country Medical Affairs Plan, collaborating with scientific leaders and cross-functional teams to enhance patient outcomes. The role involves strategic leadership, scientific engagement, and budget management within a hybrid work environment. **

Salary

Not specified; Not specified; Not specified

Skills & Requirements

Must-have

  • Country Medical Affairs Plan execution
  • Scientific engagement with key decision makers
  • Cross-functional collaboration with Marketing
  • Budget management for medical education programs
  • Regulatory compliance in medical communications

Nice-to-have

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

Key Requirements

  • Medical Knowledge and Clinical Development expertise
  • Budget Management and Strategic Planning skills
  • Regulatory Affairs Compliance experience
  • Strong Scientific Writing and Medical Review capabilities

Work Rights

Not specified

Sponsorship: available

Tailored Resume

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