pharmacovigilance

Job Description

As a Pharmacological Associate you are part of the Pharmacological Department (sometimes called the Drug Safety Department). Your role is one of reporting adverse effects (AEs) and side effects, in accordance with the current Dutch and European legislation for pharmacological. You may also train colleagues in departments such as marketing and sales, medical and clinical on how they need to comply with their reporting responsibilities for drug safety. For example, when reporting AEs it is necessary to determine what an Individual Case Safety Report (ICSR) is and establish whether the four elements of an identifiable patient, an identifiable reporter, a drug and a side effect are present during the triage-phase of a report on possible side effects. You report to your company headquarters on clinical study-related AEs and SAEs and those arising from products already on the market and any other pharmacological / product safety issues. A Pharmacological Associate (PVA) role may also be called a Pharmacological Officer, Drug Safety Officer (DOS), Drug Safety Associate, or a Patient Safety Specialist.

Keyskills :
musculoskeletal physiotherapypharmacovigilancehospital administrationhospitalitylaboratory medicineproductionphysiotherapypharma marketing