Sr Director, Patient Safety

Gilead Sciences

Eu pharmacovigilance system oversight
Deputy eu qppv responsibilities
Pharmacovigilance system master file
In this highly visible leadership role, you will partner closely with the EU QPPV and the broader Patient Safety organization to ensure our pharmacovigilance system remains robust, inspection-ready, and responsive to emerging safety needs

Job Summary

  • In this highly visible leadership role, you will partner closely with the EU QPPV and the broader Patient Safety organization to ensure our pharmacovigilance system remains robust, inspection-ready, and responsive to emerging safety needs.
  • Serve as Deputy EU QPPV in line with EU legislation, applicable EU regulations/directives, and GVP Modules; act as back-up to the EU QPPV as required.
  • This is an opportunity to make a measurable impact on patient safety at scale—helping teams navigate complex benefit–risk decisions, strengthening oversight of our pharmacovigilance system, and ensuring we meet (and exceed) expectations from regulators and stakeholders across the EEA.

Matching Summary

In this highly visible leadership role, you will partner closely with the EU QPPV and the broader Patient Safety organization to ensure our pharmacovigilance system remains robust, inspection-ready, and responsive to emerging safety needs.

Skills & Requirements

Must-have

  • EU pharmacovigilance system oversight
  • Deputy EU QPPV responsibilities
  • Pharmacovigilance System Master File
  • Risk Management Plans
  • Aggregate reports
  • Regulatory authority interactions

Nice-to-have

  • Patient-first mindset
  • Collaborative cross-functional leadership
  • Proactive safety issue management
  • Driving compliance and best practices

Key Requirements

  • Advanced medico-scientific degree
  • Significant experience leading complex work
  • Deep understanding of EU pharmacovigilance
  • MD with extensive PV/drug safety experience (preferred)

Work Rights

Not specified

Tailored Resume

Cover Letter