Job Summary
A company is looking for a Sr. Case Specialist to work remotely for an innovative pharmaceutical organization.
Key Responsibilities
- Serve as a liaison between the PV Operations team, Safety Systems Management, and the EU QPPV office to implement country-specific requirements
- Collaborate with the systems team to configure the safety database and conduct extensive testing
- Monitor and interpret regulatory intelligence for new markets to identify pharmacovigilance obligations
Required Qualifications
- Bachelor's degree in Science or a related field
- Minimum of 3-5 years of experience with global pharmacovigilance
- Hands-on experience liaising with EU QPPV and regulatory authorities
- Knowledge of global regulations (e.g., EU, MENA, LATAM, APAC)
- Experience with pharmaceutical post-market surveillance
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