Skip to main content

Research Support Ltd.

Home  About Me  Services  Contact   Testimonials   
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.