We work on Pharmacovigilance and Drug Safety jobs for some of the top global pharmaceutical, biotechnology and Clinical Services companies across the UK and Europe. Covering positions at a range of levels, including PV Compliance Managers and Drug Safety Specialist, our ambitious recruitment consultants can help place you into your next happy job!
Find out more about a career in Pharmacovigilance below, take a look at our jobs or speak with our specialist consultant Debbie Anderson for an informal chat: +44 (0)1625 541 033 / email@example.com
What is Pharmacovigilance?
Pharmacovigilance (PV or PhV) is the science and activities around drug safety. This includes the collection, detection, assessment, monitoring, reporting and prevention of adverse effects of pharmaceutical products.
Pharmacovigilance activities occur both during and post-clinical trials/product marketing. Although a medical product will have been authorised for use by the time it leaves the clinical trials phase, it will only have been tested on a small number of participants. It’s therefore vital to continue the monitoring of the product throughout its use in healthcare practice to ensure patient safety.
What does a career within Pharmacovigilance look like?
The majority of those starting out their career within Pharmacovigilance will do so in a case processing role, and will usually hold a degree within pharmacy, medical or the life sciences. These roles broadly involve inputting data from side-effects reports from patients to be evaluated by risk-management and regulatory teams.
From here, there are two typical routes to take: one into line management or a more technical route. This second option would see you working in roles such as a Risk Management Specialist or PV Scientist, within signal detection, risk management and epidemiology.
What are the typical roles within Pharmacovigilance?