Associate Director, Patient Safety Scientist V&i

AstraZeneca

Barcelona, Spain
Patient safety programs
Pharmacovigilance experience
Safety documentation authoring
This is an opportunity to further develop your pharmacovigilance (PV) experience in safety programs, spanning the entire life cycle of drug development and peri-/post-submission

Job Summary

  • This is an opportunity to further develop your pharmacovigilance (PV) experience in safety programs, spanning the entire life cycle of drug development and peri-/post-submission.
  • You will be involved in aggregating, reviewing, analyzing and interpreting safety-related data to generate information to support safety decision-making by prescribers, patients and payers, with the ultimate goal of protecting patients.
  • AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.

Matching Summary

This is an opportunity to further develop your pharmacovigilance (PV) experience in safety programs, spanning the entire life cycle of drug development and peri-/post-submission.

Skills & Requirements

Must-have

  • Patient Safety programs
  • Pharmacovigilance experience
  • Safety documentation authoring
  • Regulatory document input
  • Safety data analysis
  • Global safety strategy

Nice-to-have

  • Collaborative cross-functional work
  • Intellectual challenge
  • Scientific management approach
  • Diversity and inclusion

Key Requirements

  • 3+ years experience with Bachelor's degree
  • 2+ years experience with advanced degree
  • Clinical drug development experience
  • Post-Marketing Surveillance experience
  • MAA/BLA submissions experience
  • Periodic Safety Reports experience
  • Risk Management Plans experience
  • PV regulations knowledge
  • Handle multiple activities simultaneously

Work Rights

Not specified

Tailored Resume

Cover Letter