Pharmacovigilance scientist
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I have been involved in pharmacovigilance for over 4 years. My background is in biomedical science and I have worked in various labs including radiochemistry, diabetes and respiratory.
I am currently working as the lead pharmacovigilance scientist for multiple clients with a variety of products. Including launching a centralised license in the EU. Responsible for coordinating local Pharmacovigilance (PV) contacts across Europe, ensuring seamless communication and compliance with regulatory standards.
Timely case management activities, review of scientific literature for adverse event reports and other safety information. Responsible for authoring aggregate safety reports such as PSURs and routine safety monitoring reviews, ensuring compliance with regulatory requirements. Additionally, I manage multiple Pharmacovigilance System Master Files and Safety Management Plana to ensure completeness and accuracy.
I have an upper second class bachelors degree in Biomedical science.