Pharmacovigilance Scientist 2 (Safety Aggregate Report Specialist 2)

IQVIA

📍 Cape Town, Western Cape, South Africa 💼 Full time 🕒 Posted June 30, 2026

Apply Now Similar Jobs

Job Description

Duties/Responsibilities:
Act as signal detection and literature lead, or back-up lead to contribute to the conduct of ongoing literature safety surveillance for marketed and investigational products, evaluating events of special interests as well as aggregate data review
Author and finalize aggregate reports, including but not limited to PBRERs/PSUR, DSURs and ACOs.
Author responses to regulatory agency/ Pharmacovigilance Risk Assessment Committee (PRAC) inquiries, as required.
Can serve as principal owner (molecule lead) for the molecule and have responsibility for completion of the deliverable and in compliance with all applicable Key performance indicators (KPI); Set-up and update products' signaling strategies, as approved by the customer’s Safety Strategy Lead. Author and/or QC review all types of signal management deliverables. Lead/ conduct ongoing signal detection activities as per agreed signaling strategies, perform signal validation a...
            

Ready to Apply?

Submit your application today and join our talented team at IQVIA.

Submit Application

Job Details

Location Cape Town, Western Cape
Job Type Full time
Category Life Scientists
Posted Date June 30, 2026
Application Deadline August 09, 2026