Detects, processes and reports adverse events across a product's life.
Also known as: PV Specialist · Drug Safety Associate · DSA
PV professionals receive case reports from trials and post-market sources, code them with MedDRA, assess seriousness and expectedness, and submit ICSRs to regulators within the required windows. PSUR/PBRER aggregate authoring is the senior end of the function.
We can place a verified candidate in 2 weeks, with the dossier you actually need to make the call.