Associate Director, Patient Safety Scientist V&i

AstraZeneca

Barcelona, Spain
**
Patient safety scientist role
Global patient safety v&i team
Vaccines & immune therapies ta
** AstraZeneca is seeking an Associate Director, Patient Safety Scientist to join their Global Patient Safety team in Barcelona, Spain. The role focuses on developing safety strategies for drug development and requires a strong background in pharmacovigilance, safety documentation, and collaborative work across departments. **

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.
  • In this exciting and challenging role, you will work collaboratively with the Global Safety Physician (GSP) and other PV Scientists and physicians.
  • Our strategy and ability to transform our medicines portfolio means we have a drug-development pipeline that presents incredible opportunities to push the boundaries of science to deliver life-changing medicines.

Matching Summary

Match Score: 75

** AstraZeneca is seeking an Associate Director, Patient Safety Scientist to join their Global Patient Safety team in Barcelona, Spain. The role focuses on developing safety strategies for drug development and requires a strong background in pharmacovigilance, safety documentation, and collaborative work across departments. **

Skills & Requirements

Must-have

  • Patient Safety Scientist role
  • Global Patient Safety V&I team
  • Vaccines & Immune Therapies TA
  • Safety documentation authoring
  • Regulatory document input
  • Safety data review and analysis

Nice-to-have

  • Collaborative cross-functional interactions
  • Intellectual challenge
  • Scientific management approach
  • Commitment to doing the right thing
  • Embraces diversity and equality

Key Requirements

  • Bachelor's in sciences/pharmacy/nursing degree with 3+ years experience
  • Advanced degree with 2+ years relevant experience
  • 3+ years Patient Safety/Clinical/Drug Development experience
  • Experience in 3+ listed PV areas
  • Good knowledge of PV regulations
  • Ability to handle multiple activities simultaneously
  • Ability to work in advanced matrix structure

Work Rights

Not specified

Tailored Resume

Cover Letter