California Licensed Pharmacovigilance Specialist
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Job Summary
Providing operational support for global pharmacovigilance activities, the part-time California Licensed Pharmacovigilance Specialist will manage adverse event case processing, ensure compliance with regulatory reporting requirements, and maintain safety databases while working remotely.
Key Responsibilities:
- Process adverse event case reports and manage follow-ups for timely regulatory reporting
- Review scientific literature for safety information and prepare Periodic Safety Update Reports (PSURs)
- Maintain pharmacovigilance documentation and participate in audits and inspections
Required Qualifications:
- Bachelor's degree in Life Sciences, Pharmacy, Biology, or a related healthcare discipline
- Experience in global pharmacovigilance operations and adverse event case processing
- Knowledge of regulatory safety reporting and pharmacovigilance compliance
- Familiarity with pharmacovigilance database management and safety data review
- Advanced degree in Pharmacy, Clinical Research, Medicine, or a related healthcare field preferred
Complete Job Description
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