Job Summary
A company is looking for a Local Contact Person for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) - Freelance (English & French).
Key Responsibilities
- Act as the primary contact for local regulatory authorities regarding Pharmacovigilance and Regulatory Affairs
- Collect and report locally suspected Adverse Drug Reactions (ADRs) and manage risk minimization measures
- Prepare documentation for regulatory submissions and maintain accurate local records
Required Qualifications
- Bachelor's Degree in Life Sciences, Chemistry, Nursing, or equivalent professional experience
- Minimum 3 years of experience in the pharmaceutical or CRO industry or regulatory authority
- At least 2 years of experience in a LCPPV role or relevant pharmacovigilance position
- Pharmacovigilance training and/or relevant educational background as required by local regulations
- Proficiency in English and French, both written and verbal
Comments