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Research Support Ltd.

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Vendor Management/CRO Supervision > Project Management > Medical Writing > Clinical Trial Monitoring >  
Medical Writing


My technical writing experience includes:


  • Editing clinical trial protocols from phases I to III in a variety of therapeutic areas.
  • Preparing ethics committee submissions.
  • Writing and reviewing SOPs for sponsor and CRO clients. 
  • Writing minutes for meetings (from weekly teleconferences to large annual face-to-face meetings).
  • Devising and producing clinical trial training material.