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BIBioNTech SE

(Senior-) Director Head of Medical Review (Pharmacovigilance)(m/w/x)

Mainz, München
Full-timeOn-siteSenior

Leading a hybrid team of physicians in medical assessment of ICSRs, SUSARs, and immune-mediated events. 7-10 years pharmacovigilance experience in biotech/pharma required. Oncology expertise a plus, with Veeva Vault Safety proficiency.

Requirements

  • Medical or advanced life sciences degree; PhD or post-graduate training in pharmacovigilance preferred
  • 7–10 years pharmacovigilance experience in biotech or pharmaceutical industries; oncology expertise advantageous
  • Leadership experience as Medical Review Lead or similar for Senior Director consideration
  • Comprehensive knowledge of global pharmacovigilance regulations (ICH, GVP) and hands-on ICSR processing experience
  • Proficiency in safety databases such as Veeva Vault Safety
  • Strong communication skills with ability to convey complex concepts clearly
  • Excellent English skills

Tasks

  • Lead and mentor a hybrid team of medical review physicians
  • Oversee high-quality medical assessments of ICSRs
  • Focus on critical cases like SUSARs, immune-mediated events, and pDILI
  • Drive continuous improvement in medical review processes
  • Provide expert guidance on ICSR assessments
  • Establish SOPs for consistent medical case reviews
  • Collaborate with Global Clinical Development and Quality
  • Manage vendor relationships and performance
  • Ensure alignment with global regulatory standards
  • Foster an environment of accountability and innovation

Work Experience

  • 7 - 10 years

Education

  • Bachelor's degree

Languages

  • EnglishNative

Tools & Technologies

  • Veeva Vault Safety
  • ICH
  • GVP
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