Your newpany

We are supporting a leading global biopharmaceutical organisation in the search for a Pharmacovigilance Quality Document Associate to join their Safety function on a 12-month contract.This is a hybrid, ideally 2 days in the office (Berkshire), but there is some flexibility.This opportunity is ideal for candidates with strong quality control (QC) experience with aggregate safety reports (, PSURs, DSURs) and exceptional scientific editing skills, rather than a background focused primarily on case processing.

Your new role

You will be responsible for performing rigorous QC reviews of pharmacovigilance documents, ensuring the highest standards of accuracy, consistency, andpliance across Safety Surveillance and Aggregate Reporting outputs.You will also contribute to process improvement initiatives, vendor oversight, and quality standards development, making this a highly collaborative and impactful role within the PV quality space.

What you'll ne...