Stage- Pharmacovigilance

AstraZeneca

France
Pharmacovigilance case validation
Regulatory reporting to authorities
Signal detection and review
The role involves collecting, validating, and evaluating suspected adverse drug reaction notifications within the French subsidiary of AstraZeneca

Job Summary

  • The role involves collecting, validating, and evaluating suspected adverse drug reaction notifications within the French subsidiary of AstraZeneca.
  • Candidates will be responsible for registering cases in local databases and declaring them to health authorities within required legal timeframes.
  • The position includes participating in signal detection, reviewing periodic safety reports, and contributing to medical information regarding product safety.

Matching Summary

The role involves collecting, validating, and evaluating suspected adverse drug reaction notifications within the French subsidiary of AstraZeneca.

Skills & Requirements

Must-have

  • pharmacovigilance case validation
  • regulatory reporting to authorities
  • signal detection and review
  • medical information support
  • product complaint handling

Nice-to-have

  • bibliographic surveillance skills
  • clinical study protocol writing
  • periodic safety report drafting
  • collaboration with quality assurance
  • comittees on good usage participation

Key Requirements

  • Knowledge of pharmacovigilance regulations
  • Experience with clinical trial data
  • Ability to draft safety reports

Work Rights

Not specified

Tailored Resume

Cover Letter