CK Group are currently recruiting for someone on a permanent basis to join a global CRO as a Senior Clinical Safety Coordinator.
Responsibilities of the role:
- Collect, process, and track serious adverse event (SAE) reports
- Safety Database data entry
- Perform quality control of safety cases
- SAE reconciliation between safety database and clinical database
- Leading clinical trial projects- ensuring client deliverables are met, providing oversight and compliance reports
Qualifications needed:
- Bachelor?s life science degree
- Experience in Pre-Market Clinical Trial Pharmacovigilance (4+ years)
- Working knowledge of Safety Databases (Argus is desirable)
- Demonstrate advanced knowledge of medical terminology, global safety reporting requirements and Good Clinical Practice (GCP) Guidelines
- Exposure to working on global trails as part of a multidisciplinary team
This role offers a good salary, with the opportunity to develop into a managerial position which also has a great working culture, however requires for the candidate to be fully office present for the first 6 months of starting the position, which then changes to 8 times a month which can be structured with flexibility. Their offices are based in London and Stirling.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 54998 in all correspondence.
You must have the right to work in the UK. Learn more
- Agency: CK Group
- Reference: 54998
Website: CK Group
- Posted: 14th March 2023
- Expires: 11th April 2023
