Pharmacovigilance Services Specialist

Accenture

Pharmacovigilance services - safety writing
Pbrer and rmp process
Aggregate reports and rmp documents
Manage and develop individual case narratives describing adverse events for inclusion in regulatory submissions and safety reports

Job Summary

  • Manage and develop individual case narratives describing adverse events for inclusion in regulatory submissions and safety reports.
  • Ensuring the aggregate reports and RMP documents are medically relevant, complete, consistent and accurate.
  • Responsible for knowledge sharing, coaching, review and providing feedback of reports medically analyzed by the mentees.

Matching Summary

Manage and develop individual case narratives describing adverse events for inclusion in regulatory submissions and safety reports.

Skills & Requirements

Must-have

  • Pharmacovigilance Services - Safety Writing
  • PBRER and RMP process
  • aggregate reports and RMP documents
  • medical analysis for AR and RMP
  • knowledge sharing and coaching

Nice-to-have

  • converging around the patient
  • connecting scientific expertise
  • unique insights into patient experience

Key Requirements

  • MBBS/MD
  • 3 to 8 years of experience
  • Minimum 3 years of experience in PBRER and RMP process
  • English(Domestic) - Expert

Work Rights

Not specified

Tailored Resume

Cover Letter