Freelance QPPV - European/UK Pharmacovigilance Lead

Clinigen; Eu; Hybride; EUR 20 000 - 40 000; Temps partiel

Résumé du poste

A specialised pharmaceuticals company is seeking a freelance Qualified Person for Pharmacovigilance (QPPV) to join their network in France. The ideal candidate will have over 7 years of experience in pharmacovigilance, strong knowledge of regulations, and proven abilities in managing safety reporting and compliance. This role supports various clients, ensuring that safety issues are effectively managed in accordance with EU and UK laws.

Qualifications

• 7+ years of experience in pharmacovigilance.
• Documented experience in management of PV systems.
• Experience in audits and regulatory inspections.

Responsabilités

• Act as QPPV for compliance with EU and UK legislation.
• Oversee pharmacovigilance activities and safety issues.
• Submit safety reports to regulatory authorities.
• Maintain the pharmacovigilance system and safety databases.

Connaissances

Experience as a QPPV

Knowledge of PV legislation

Analytical thinking

Effective communication

Collaboration with stakeholders

Fluency in English

Knowledge of MS Office Applications

Formation

Life Science Degree

Medical degree (preferred)

Description du poste

A specialised pharmaceuticals company is seeking a freelance Qualified Person for Pharmacovigilance (QPPV) to join their network in France. The ideal candidate will have over 7 years of experience in pharmacovigilance, strong knowledge of regulations, and proven abilities in managing safety reporting and compliance. This role supports various clients, ensuring that safety issues are effectively managed in accordance with EU and UK laws.