This independent contract research organisation focusses on several professional services, such as: regulatory support, clinical studies, PV services and quality assurance activities for a multitude of well-known clients all over the world. Within this spectrum they are experiencing a strong growth and as a result are currently on the look-out for a skilled and experienced Qualified Person in Pharmacovigilance (QPPV).
In this exciting role you have complete oversight of the organisation’s pharmacovigilance systems as well as the systems of its clients. In addition you will ensure 24/7 availability for the safety of medicinal products and medical devices. Responsibilities such as keeping overview of medicinal product safety profiles and emerging safety concerns also belong to your job scope. Also you will be executing the QPPV function within the company and globally, ensuring constant compliance with European PV legislation and European regulations. This all the while building strong working relationships with local Drug Safety Officers in EU countries.
In order to be eligible for this role, the following qualifications and skills apply to you:
Besides a stimulating, fast growing and dynamic working environment the company offer the following to you:
If you are interested in this job, or in similar ones, please feel free to contact me directly.
Martin van der Velden
Consultant Clinical Research & Medical Affairs | Biotechnology