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-Library | £30,000 / Year Directive, Medical Device Directive, UK Clinical Trials Regulations, Principles 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. - Working knowledge of BS EN ISO
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