Talentmark is recruiting a Clinical Development Lead on a 12-month contract. The role is hybrid with 3 days on-site in Burgess Hill and two days remote.
You will lead documentation strategy to support regulatory submissions and liaise with Clinical Development Leaders, Regulatory, Quality, Labelling and R&D. You will author, review and finalise critical documents including IVDR Performance Evaluation materials, protocols, CSRs and Investigator Brochures, and conduct literature reviews to
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For the Hybrid Clinical Development Lead – Regulatory Documentation position at Talentmark, we are reviewing applications now.
All applications are reviewed carefully by our team.
The position is based in Hurstpierpoint, England, United Kingdom.
This opportunity is part of our work in Bio & Pharmacology & Health, IT & Technology.
The advertised compensation is 69.000 - 119.000.
We aim to respond to suitable candidates as soon as possible.