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

Parexel; Berlin; Remote; EUR 70.000 - 100.000; Vollzeit

Zusammenfassung

Parexel is seeking Local Qualified Persons for Pharmacovigilance (QPPV) freelancers to join their network for future projects. This role, adaptable to remote work from select EMEA locations, focuses on ensuring compliance with global PV regulations and managing safety risk effectively.

Qualifikationen

• Minimum 7 years' experience managing or implementing PV systems.
• Documented experience in pharmacovigilance.
• Extensive knowledge of GVP and GCP guidelines.

Kenntnisse

Expert knowledge of local PV legislation

Pharmacovigilance safety risk management

Global pharmacovigilance regulations

Jobbeschreibung

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

Client:

Parexel

Location:

Berlin, Germany

Job Category:

Other

EU work permit required:

Yes

Job Reference:

6a2c363ab5e8

Job Views:

3

Posted:

23.06.2025

Expiry Date:

07.08.2025

Job Description:

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

Parexel is dedicated to improving global health through biopharmaceutical services that transform scientific discoveries into new treatments. Our offerings include clinical trials, regulatory affairs, consulting, and market access, all driven by our core values: Patients First, Quality, Respect, Empowerment, and Accountability.

The Pharmacovigilance team is seeking to build a network of Local Qualified Person for Pharmacovigilance (QPPV) freelancers for future projects.

This role can be performed remotely in select EMEA locations and Australia.

Requirements

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

Please note: If you are not a passport holder of the country for the vacancy, you might need a work permit. Check our Blog for more information.

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