Manager Drug Safety Physician

Cencora

Development and authorship of safety reports
Tracking of commitments and liaising with functions
Medical review of aggregate safety reports
Develop, author, and track Safety Reports (PSUR/RMP/ACOs) ensuring high quality and regulatory compliance

Job Summary

  • Develop, author, and track Safety Reports (PSUR/RMP/ACOs) ensuring high quality and regulatory compliance.
  • Oversee service performance, mentor employees, and manage logistical aspects for timely development of safety reports.
  • Provide expertise for finalization of safety reports, resolve issues, and develop product-specific training materials.

Matching Summary

Develop, author, and track Safety Reports (PSUR/RMP/ACOs) ensuring high quality and regulatory compliance.

Skills & Requirements

Must-have

  • Development and authorship of Safety Reports
  • Tracking of commitments and liaising with functions
  • Medical review of Aggregate Safety reports
  • Signal detection and characterization of safety concerns
  • Knowledge of safety databases and regulatory guidelines

Nice-to-have

  • Collaborative mindset and strong interpersonal skills
  • Proactive problem-solving approach
  • Exposure to corporate pharmaceutical environments

Key Requirements

  • Minimum 5-7 years of pharmacovigilance experience
  • Degree in Medicine (MBBS / MD required)
  • Hands-on experience in medical review of Aggregate Safety reports
  • Proficiency in global regulatory frameworks and GxP compliance

Work Rights

Not specified

Tailored Resume

Cover Letter