Clinical Safety And Risk Management Associate Principal Scientist

Merck Sharp & Dohme Corp

Hybrid
Medical review of adverse events
Pharmacovigilance and risk management
Strong written and verbal communication
You will play a critical role in protecting patient safety by actively monitoring, assessing, and communicating the safety profile of our medicines

Job Summary

  • You will play a critical role in protecting patient safety by actively monitoring, assessing, and communicating the safety profile of our medicines.
  • You will perform medical and scientific review of adverse event data and work closely with CSRM physicians to identify and manage safety risks.
  • Your contributions to safety surveillance and regulatory deliverables are key in ensuring patient safety.

Matching Summary

You will play a critical role in protecting patient safety by actively monitoring, assessing, and communicating the safety profile of our medicines.

Skills & Requirements

Must-have

  • Medical review of adverse events
  • Pharmacovigilance and risk management
  • Strong written and verbal communication

Nice-to-have

  • Subject matter expertise in risk management
  • Experience with safety databases
  • Ability to analyze complex safety data

Key Requirements

  • Medical Doctor (MD)
  • Minimum 5 years of relevant experience
  • At least 2 years in drug safety or pharmacovigilance

Work Rights

Not specified

Tailored Resume

Cover Letter