Local Qualified Person for Pharmacovigilance (QPPV) Freelancer - TALENT POOL

Parexel; Paris; Hybride; EUR 80 000 - 120 000; Temps partiel

Résumé du poste

A leading biopharmaceutical company in France is looking for a Local Qualified Person for Pharmacovigilance (QPPV) Freelancers. This remote role requires at least 7 years of experience in pharmacovigilance and expert knowledge of local PV legislation. The candidate will manage PV systems and ensure compliance with global regulations.

Qualifications

• Minimum of 7 years' experience in managing PV systems.
• Documented experience in all aspects of PV to fulfill Local QPPV responsibilities.

Connaissances

Expert knowledge of local PV legislation

Experience in quality assurance

Knowledge of global pharmacovigilance regulations

Experience in safety risk management

Description du poste

Overview

When our values align, there's no limit to what we can achieve.

Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do.We believe in our values; Patients First, Quality, Respect, Empowerment & Accountability.

The Pharmacovigilance team are looking to build a network of Local Qualified Person for Pharmacovigilance (QPPV) FREELANCERS for future projects.

The role can be based remo t ely in select EMEA locations and Australia.

Qualifications

• Expert knowledge of local PV legislation in territory(ies) where assigned as the Local QPPV
• Minimum of at least 7 years' demonstrated experience in managing or implementing PV systems, including quality assurance experience
• Documented experience in all aspects of PV in order to fulfill the responsibilities of the Local QPPV.
• Extensive knowledge of global pharmacovigilance regulations and GVP and GCP guidelines
• Experience in pharmacovigilance safety risk management including clinical trials, post-market pharmacovigilance, safety case processing, safety reporting, and safety systems