Pharmacovigilance Coordinator

PPD (Thermo Fisher)

UK
Protocol inquiry review
Adverse event tracking
Dsmb meeting coordination
The role involves coordinating serious and non-serious adverse events alongside protocol inquiries for global pharmaceutical programs

Job Summary

  • The role involves coordinating serious and non-serious adverse events alongside protocol inquiries for global pharmaceutical programs.
  • Candidates will represent the organization at Data Safety Monitoring Board meetings and manage all logistical aspects of these committees.
  • The position requires maintaining audit-ready program files and ensuring strict adherence to FDA Regulations and ICH Good Clinical Practices.

Matching Summary

The role involves coordinating serious and non-serious adverse events alongside protocol inquiries for global pharmaceutical programs.

Skills & Requirements

Must-have

  • protocol inquiry review
  • adverse event tracking
  • DSMB meeting coordination
  • contractual document preparation
  • MS Office proficiency
  • FDA regulations knowledge

Nice-to-have

  • strong problem solving skills
  • ability to work independently
  • effective oral communication
  • positive professional demeanor
  • flexibility to reprioritize workload

Key Requirements

  • High school diploma or equivalent
  • At least 2 years relevant experience
  • Knowledge of FDA Regulations and ICH GCP

Work Rights

Not specified

Tailored Resume

Cover Letter