Drug Safety/Pharmacovigilance is the practice of monitoring and preventing adverse effects in Patients within clinical trial and marketed products.
This is commonly viewed in two ways. Firstly the reporting, triaging and expediting of adverse events this is commonly run through Drug Safety Centres covering case processing.
Secondly the investigation and prevention of further adverse events. This is commonly covered within Risk Management and Signal detection teams.
The types of positions we have successfully recruited for across pharma, biotech and medical devices are;
- PV Auditor
- VP/Director Pharmacovigilance/Drug Safety
- Risk Management Physician
- Pharmacovigilance Physician
- Pharmacovigilance Scientist
- Drug Safety Manager/Associate
- Aggregate Report Writer
For more information on anything we may be able to help you with please call one of our experienced consultants on +44 (0) 2085443400 London or +00 1 857 305 6572 Boston