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UK Based Freelance EU IVD Regulatory Affairs Consultant - United Kingdom - RBW Consulting
Description
UK Based Freelance EU IVD Regulatory Affairs Consultant
RBW Consulting are working in partnership with a global mid-sized CRO in their search for a Freelance IVD Regulatory Affairs Consultant based in the EU to start as soon as possible within their IVD function.
Local ethics committee submissions and Annex XIV submissions for clinical trial assay across the majority of EU member states within the past 2 yearsExperience with reviewing and assembling the clinical trial documentation for the regulatory submissions including protocols, IB, ICF, CRF to competent authorities
Working knowledge and experience within an IVD Regulatory Affairs function Reach out to find out more
Apply for UK Based Freelance EU IVD Regulatory Affairs Consultant
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