Job Summary
A company is looking for a Global Drug Safety Senior Case Specialist.
Key Responsibilities
- Monitor and interpret regulatory intelligence for pharmacovigilance obligations in new markets
- Translate regulatory requirements into actionable configuration needs for safety databases
- Collaborate cross-functionally to ensure alignment with global pharmacovigilance systems and processes
Required Qualifications
- Bachelor's degree in life sciences, pharmacy, or related field
- 3+ years of pharmacovigilance operations experience, particularly in global expansion
- Familiarity with safety databases and regulatory reporting requirements across multiple regions
- Experience with quality management systems and inspection readiness principles
- Hands-on experience with Veeva Vault or similar modules
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