Pharmacovigilance Liaison Scientist
CY Partners have an exciting opportunity for a Pharmacovigilance Liaison Scientist to join a leading global pharmaceutical organisation, based in Brentford. This opportunity will be home working initially, with flexible working arrangements long term.
As liaison scientist, you will be ensuring the safety of all Clinical Trial participants and patients administered products, by ensuring the successful collection, assessment and reporting of safety data (adverse events).This role ensures that case processing activities align with company standards for processing HSI and that regulatory timelines are achieved. This is done by liaising with global stakeholders (both internal and external).
As Liaison Scientist, you will provide the relevant liaison-related oversight to the Case Management Group (CMG) Directors and drive the understanding of adverse event collection requirements across all business units.
Previous experience of Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), clinical safety documentation, reporting of adverse events from clinical trials, local regulatory requirements, and pharmacovigilance methodology would be highly desirable.
Get in touch with Helen at CY Partners on 07851246847, for a confidential chat about the role or apply by sending across your CV to [email protected]