The role of a Sr European Regulatory Database Associate/Pharmacovigilance Associate is twofold. Evenly divided you will act as a Regulatory Database Associate and as a Pharmacovigilance Associate.
As a Regulatory Database Associate, you ensure a high standard of data integrity for the following region: Europe/Africa/Middle East. Therefor you identify, prioritise & resolve issues relating to RA. You will also train & support in-country RA Managers and VMRA's.
As a Pharmacovigilance Associate you will, amongst other tasks, keep track of PSUR line lists, import and process Adverse Event cases.