Senior Clinical Safety Coordinator - London, United Kingdom - CK GROUP
Description
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
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
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 54998 in all correspondence.
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