Freelance Regulatory Affairs Consultant

2 weeks ago


England, United Kingdom RBW Consulting Full time

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



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