Sr. Specialist Medical Affairs (temporary)

Merck & Co., Inc.

Rahway, NJ, USA
Not specified; not specified; not specified
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 and non-interventional research studies in compliance with Good Pharmacoepidemiology Practice

Job Summary

  • This position is responsible for the end-to-end operational execution of observational and non-interventional research studies in compliance with Good Pharmacoepidemiology Practice.
  • The role involves coordinating vendor documents, managing study timelines, and supporting the preparation of protocols, reports, and scientific publications.
  • Candidates must possess a Bachelor's degree in a health-related science 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 and non-interventional research studies in compliance with Good Pharmacoepidemiology Practice.

Salary

Not specified; Not specified; Not specified

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 on diverse stakeholders

Key Requirements

  • Bachelor's degree in Nursing, Biology, Public Health, or related science
  • 2+ years of work experience in clinical/observational research
  • Advance English written and spoken proficiency

Work Rights

Not specified

Tailored Resume

Cover Letter