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 years
✔ Experience 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!
+44 (0)1293 364 092
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