Associate Director Patient Safety Scientist

AstraZeneca

Mölndal, Sweden
**
Patient safety experience
Clinical drug development
Post-marketing surveillance
** AstraZeneca is seeking an Associate Director Patient Safety Scientist in Mölndal, Sweden, to enhance patient safety through proactive pharmacovigilance and risk management. The role involves collaboration with cross-functional teams to evaluate safety data and author regulatory documents, requiring a life sciences degree and extensive experience in patient safety. **

Job Summary

  • The core purpose of AstraZeneca Patient Safety is to add value to AstraZeneca products, provide clear science-based guidance for investigators and prescribers to safeguard patients as well as the success of our business.
  • You work with Patient Safety Physicians and other PS Scientist(s) with review, analysis and interpretation of safety data obtained from patients who have been administered the assigned medicinal products in clinical development programs and/or from marketed use.
  • We balance the expectation of being in the office while respecting individual flexibility.

Matching Summary

Match Score: 75

** AstraZeneca is seeking an Associate Director Patient Safety Scientist in Mölndal, Sweden, to enhance patient safety through proactive pharmacovigilance and risk management. The role involves collaboration with cross-functional teams to evaluate safety data and author regulatory documents, requiring a life sciences degree and extensive experience in patient safety. **

Skills & Requirements

Must-have

  • Patient Safety experience
  • Clinical drug development
  • Post-Marketing Surveillance
  • Periodic Safety Reports
  • Risk Management Plans
  • Pharmacovigilance regulations
  • Written and verbal English

Nice-to-have

  • Entrepreneurial mindset
  • Thinking big
  • Working together
  • Integrity
  • Doing the right thing
  • High-performing learning organization

Key Requirements

  • Life sciences/pharmacy/nursing degree
  • At least 2 years of Patient Safety experience in specified areas
  • Intermediate pharmacovigilance regulations knowledge
  • Fluent in written and verbal English

Work Rights

Not specified

Tailored Resume

Cover Letter