Pharmacovigilance Regulatory Affairs Specialist

A company is looking for a Local Contact Person for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) - English & French. Key Responsibilities Act as the primary contact with local regulatory authorities for Pharmacovigilance and Regulatory Affairs Manage local reporting of adverse drug reactions and oversee risk minimization measures Prepare documentation for regulatory submissions and ensure compliance with local regulations Required Qualifications Bachelor's Degree in Life Sciences, Chemistry, Nursing, or equivalent 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 Expert knowledge of ICH GVP and local regulatory requirements

Jun 5, 2025 - 18:50
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Pharmacovigilance Regulatory Affairs Specialist
A company is looking for a Local Contact Person for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) - English & French. Key Responsibilities Act as the primary contact with local regulatory authorities for Pharmacovigilance and Regulatory Affairs Manage local reporting of adverse drug reactions and oversee risk minimization measures Prepare documentation for regulatory submissions and ensure compliance with local regulations Required Qualifications Bachelor's Degree in Life Sciences, Chemistry, Nursing, or equivalent 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 Expert knowledge of ICH GVP and local regulatory requirements