Global Safety Lead - Formulation Safety

CSL SEQIRUS

Multiple Locations
On-site
Clinical safety expertise
Safety risk management
Pharmacovigilance tasks
CSL Seqirus is seeking a Global Safety Lead for Formulation Safety, responsible for overseeing clinical safety throughout the product lifecycle, including risk management and safety strategy in cross-functional teams. The ideal candidate will possess an MD or equivalent, with significant experience in the pharmaceutical industry, particularly in clinical safety and risk management

Job Summary

  • The Director, Global Safety Lead, Formulation Safety provides expertise on all aspects of clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and post approval.
  • The role serves as the safety representative in the cross-functional development teams and post-marketing product teams, responsible for setting safety strategy for global projects.
  • CSL Behring is a global biotherapeutics leader driven by its promise to save lives, focused on serving patients' needs by using the latest technologies.

Matching Summary

Match Score: 85

CSL Seqirus is seeking a Global Safety Lead for Formulation Safety, responsible for overseeing clinical safety throughout the product lifecycle, including risk management and safety strategy in cross-functional teams. The ideal candidate will possess an MD or equivalent, with significant experience in the pharmaceutical industry, particularly in clinical safety and risk management.

Skills & Requirements

Must-have

  • clinical safety expertise
  • safety risk management
  • pharmacovigilance tasks
  • signal detection and evaluation
  • regulatory agency requests

Nice-to-have

  • proactive risk mitigation
  • cross-functional team representation
  • strong product knowledge

Key Requirements

  • MD or international equivalent plus accredited residency
  • Two (2) years minimum experience as a physician in patient care
  • 3+ years pharmaceutical/biotechnology industry experience
  • 1 year medical oversight/evaluation or clinical development
  • Industry experience in designated therapeutic area(s)

Work Rights

Not specified

Tailored Resume

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