Clinical Safety Scientist
Clinical Life Sciences Pharmaceuticals
CY partners are working on an exciting opportunity for a clinical safety scientist to join a world leading global pharmaceutical organisation. The role offers a mix of home based and office working at their site in Brentford and is available initially on a 6-month contract basis.
The key purpose of this role is to ensure the safety of all Clinical Trial participants, patients, and consumers administered or using the organisations products, by supporting the successful collection, processing and reporting of safety data (adverse events) of GSK products globally.
This role ensures that case management activities align with company standards for processing human safety information (HSI) and that regulatory requirements, including timelines are achieved. This is done by liaising with global stakeholders (both internal and external), managing case processing activities and overseeing the PV case processing vendor. The job holder provides relevant ICSR Management-related oversight to the Case Management Group (CMG) Directors and drives the understanding of adverse event collection requirements across all business units.
Discuss the role further with Helen Tomlinson at CY Partners on 07851246847 or apply with your CV to [email protected]