Sr. Specialist Medical Affairs (temporary)

Merck & Co., Inc.

Hybrid
Observational research study execution
Good pharmacoepidemiology practice compliance
Vendor document coordination
This position is responsible for the end-to-end operational execution of observational research studies in compliance with Good Pharmacoepidemiology Practice

Job Summary

  • This position is responsible for the end-to-end operational execution of observational research studies in compliance with Good Pharmacoepidemiology Practice.
  • The role involves coordinating vendor documents, tracking study timelines, and managing the development of medical publications and posters.
  • Candidates must have a Bachelor's degree in a health-related discipline and at least two years of experience in clinical or observational research.

Matching Summary

This position is responsible for the end-to-end operational execution of observational research studies in compliance with Good Pharmacoepidemiology Practice.

Skills & Requirements

Must-have

  • observational research study execution
  • Good Pharmacoepidemiology Practice compliance
  • vendor document coordination
  • study timeline tracking
  • medical writing and publication development

Nice-to-have

  • strong project management skills
  • ability to work independently
  • collaboration with cross-functional teams
  • understanding of digital innovation
  • influence over diverse stakeholders

Key Requirements

  • Bachelor's degree in Nursing, Biology, Public Health, or science
  • 2+ years of work experience in clinical/observational research
  • Advance English written and spoken proficiency
  • Project Management Professional or Certified Associate Project Management certification (Preferred)

Work Rights

Not specified

Tailored Resume

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