Director/Senior Director, Safety-PV Operations Lead

Added
25 minutes ago
Type
Full time
Salary
Salary not provided

Related skills

veeva argus 21 cfr part 11 gvp meddra
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πŸ“‹ Description

  • Provide strategic direction for global safety and pharmacovigilance operations.
  • Develop and oversee safety documents and partner agreements (JOGs, Safety Plans, DSAs).
  • Coordinate core safety docs (DSURs, Reference Safety Info, RMP/REMS materials) with Regulatory
  • Coordinate safety outputs with Biostatistics, QA, medical writing, vendors.
  • Support ongoing safety surveillance, including signal management and risk assessment.
  • Act as primary contact for safety vendors and CROs; manage budgets and deliverables.

🎯 Requirements

  • Advanced degree such as PhD, PharmD, MSc, or equivalent in life-science/medical field.
  • 5+ years in pharmacovigilance/safety operations leadership across biotech and pharma.
  • Experience supporting late-stage development, commercialization, and expanded-access programs.
  • In-depth knowledge of global PV/safety requirements (GVP, 21 CFR Part 11).
  • Strong understanding of pre/post-marketing safety and regulatory expectations.
  • Experience creating/maintaining CCSI and RMP/REMS docs.

🎁 Benefits

  • Full-time, remote position with flexible working environment.
  • Opportunity to work with international teams across Europe, North America, and Israel.
  • Flexible schedule for multiple time zones.
  • Opportunity to contribute to late-stage clinical development and commercialization programs.
  • Significant ownership and strategic influence over global safety ops.
  • Occasional travel for in-person collaboration.
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