Experiencing medical writing

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Course features
  • Author: Sarah Tilly
  • Level: Advanced
  • Study time: 100 hours
  • Video time: 5 hours
  • Assessments: 3
  • Written feedback: 2
  • 1-to-1 live feedback: 2 hours
  • Certification: if 60% + upon assignment update
Course overview
Understand how medical writers assist with a wide range of clinical trial documents, from the protocol at the planning stage through to a journal article to disseminate reasearch findings to the wider community. View real documents, understand the correct guidelines to follow, and receive individual written and verbal feedback from your reviewer. Learn how to improve your work, update, and resubmit for final assessment.
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COURSE OBJECTIVES
Learn in-depth about clincal trials and how medical writers  contribute 
Write a full assignment as if you were a real medical writer - view and use real clinical documents
Receive valued written and verbal feedback from experts

What's included?

Meet the instructor

Sarah Tilly

Sarah values people, from patients to team members. She believes that everyone has their own, unique contribution to give to our industry. For this reason, she has been involved in mentoring new medical writers since an early stage of her career. In parallel with her largely regulatory writing experience, she has managed and mentored several teams of writers and has been involved in setting up and coordinating training systems. At Azur Health Science, she is  actively involved in advising and mentoring other writers. Sarah has been medical writing since 2006 in clinical research organisations and medical writing consultancies. She set up Azur Health Science in 2017 as Medical Writer and Director. She holds a first degree in Biology and a PGCert in International HTA, Pricing and Reimbursement. 
      (No, she does not have a PhD!).
Patrick Jones - Course author
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