Global Safety Program Lead - Cell Therapy Oncology & Onco-hematology

AstraZeneca

Barcelona, Spain
Base: $288,059.20 - $432,088.80 usd; bonus/equity:...
Medical degree or equivalent in biomedicine
Extensive clinical safety and pharmacovigilance experience
Deep knowledge of global pv regulations and standards
This role offers the opportunity to shape the safety strategy for high-impact cell therapy assets across pre-clinical, clinical, and post-marketing stages

Job Summary

  • This role offers the opportunity to shape the safety strategy for high-impact cell therapy assets across pre-clinical, clinical, and post-marketing stages.
  • The successful candidate will lead a team of safety physicians and scientists while ensuring compliance with Good Clinical and Pharmacovigilance Practice.
  • AstraZeneca provides a competitive compensation package including base pay ranging from $288,059.20 to $432,088.80 USD, along with equity incentives and comprehensive health benefits.

Matching Summary

This role offers the opportunity to shape the safety strategy for high-impact cell therapy assets across pre-clinical, clinical, and post-marketing stages.

Salary

Base: $288,059.20 - $432,088.80 USD; Bonus/Equity: Short-term incentive bonus and equity-based long-term incentive program available; Benefits: Qualified retirement program (401k), paid vacation/holidays, leaves, medical/dental/vision coverage

Skills & Requirements

Must-have

  • Medical degree or equivalent in biomedicine
  • Extensive clinical safety and pharmacovigilance experience
  • Deep knowledge of global PV regulations and standards
  • Proven track record leading asset safety strategy
  • Strong matrix leadership and cross-functional influencing skills

Nice-to-have

  • PhD or advanced degree in relevant scientific discipline
  • Research experience in Cell and Gene Therapy field
  • Medical specialty in oncology or haemato-oncology
  • Experience speaking at industry conferences
  • Knowledge of PV regulations in China, Australia, Japan

Key Requirements

  • Medical degree or equivalent in biomedicine or science
  • Extensive clinical safety/pharmacovigilance experience spanning pre- and post-launch
  • Demonstrated strategic influence on clinical studies and benefit-risk decisions
  • Ability to travel domestically and internationally as business needs require

Work Rights

Not specified

Tailored Resume

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