20 November 2020

AUTHOR: David Boyd

Job Title: EEA QPPV
Reports to: Technical Director
Location: Dublin and/or locations in Northern Europe (Lille, Paris, Bruxelles, Amsterdam, Rotterdam, Copenhagen, Malmo, Stockholm, Berlin)

Role Overview

Diamond PV provides pharmacovigilance services to wide range of clients from Clinical Trials to Post Marketing, and from single product/single market through to global reach with >30 products. Products we support include COVID-19 vaccines undergoing clinical trials, end-to-end PV support for gene therapies through to post marketing PV of generic products.

In most cases, Diamond acts as a fully outsourced PV provider, acting as our client’s inhouse PV team and providing a full PV system including QPPV, safety database, medical writing and case processing.

Due to increasing demand from our current clients, we are recruiting two additional EEA QPPVs to support our existing QPPV team. These will be based either in our Dublin office, or remotely in a Northern European city. Diamond’s systems are fully electronic and paperless, allowing seamless remote working from any location.

The EEA QPPV is a mandated business critical regulatory and safety governance role with broad responsibilities as defined by European legislation.

Skills & Experience

Applicants will require a science degree and prior experience as a QPPV or Deputy QPPV.

Skills & experience we are looking for include:

  • Expert understanding of all area of pharmacovigilance
  • A positive pragmatic outlook on all matters
  • Strong communication skills
  • Effective decision maker
  • Able to delegate effectively
  • A minimum of 7 years experience of working in Pharmacovigilance
  • Experience of both PM and CT is desirable
  • Experience in novel therapies, cell therapy and gene therapy is desirable

If you are keen on joining this exciting, forward thinking company and taking the next step in your career, then please contact us now to find out more.