25/04/2024 | Fulltime | Bristol | CV-Library | £45,000 / Year Of ICH-GCP, GDPR and Research Governance Framework Legislation with proven ability to apply these to the coordination of clinical trials. - Understanding of current EU Medical Device Regulation. - Evidence of preparing regulatory and ethics submissions, writing/amending Clinical Investigation Plans
Save for laterRegister your CV15/04/2024 | Fulltime | Bristol | CV-LibraryAssociate Risk Manager Due to such a large pipeline of work in the Specialist portfolio, it is essential that applicants in this role have a proven track record working as a Risk Manager in an engineering environment. This can be working with a client, consultancy, or contractor in sectors
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