Regulatory Affairs and Pharmacovigilance Expert

3 days ago


London, Greater London, United Kingdom EPM Scientific Full time
Key Responsibilities
  • Coding safety events using MedDRA terminology, data entry in the Pharmacovigilance Database, and AE monitoring
  • Producing safety data for signal detection and periodic aggregate reports, and providing safety information to the regulatory department
  • Assisting in improving the pharmacovigilance system, ICSR and SUSAR reporting, and Medical and Scientific Literature searches

Salary Range: £50,000 - £60,000 per annum

Additionally, we offer a competitive package with benefits, opportunities for professional growth, and the chance to collaborate with world-leading scientific experts.



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