As a Case Processor you will be responsible for entry and the evaluation and assessment of case reports for seriousness, global listedness and causality of all serious and non-serious adverse events.
Structured entry of serious and non-serious adverse events onto Client’s global PV safety database according to Client’s User Manual.
Extraction of relevant information from routine source documents and/or information coming from the Client affiliates via the LAM or from E2B messages
Preliminary evaluation and assessment of case reports for seriousness, global listedness and causality of all serious and non-serious adverse events
Accurate and timely AE/SAE data entry taking into account the automated case prioritization by Client’s global PV database and timely processing of action items considering the system-generated due dates for completion.
Creation of comprehensive case descriptions (narratives) in English language extracting relevant PV information from routine source documents
Checking of incoming PV information for consistency and completeness
Verification of the accuracy of MedDRA and WHO-DD coding of reported adverse events, concomitant drugs
Bachelor of Science in Biological Sciences ( Bachelor in Allied Health, BSc Public Health, BSc Human Nutrition, Bachelor in Public Health, Bachelor in Pre-Medicine, Nursing Degree, Pharmacist)
0 to 2 years of relevant experience in Case processing/ Pharmacovigilance