Medical Writer

St. Petersburg, Moscow, Kyiv
2 years
Contract, full-time

Main responsibilities of a Medical Writer include:

  • Developing study design, including determining sample size
  • Consulting customers at the stage of developing study documentation
  • Creating the above-mentioned study documents
  • Consulting the study team on study protocol related questions.


  • Degree in Medicine or Biology; PhD or Dr of Medical Sciences Experience in writing essential documents (including study protocols, subject consent forms, investigator brochures, IMPDs, final study reports, CRF, etc) for EMEA or/and FDA clinical trials
  • Knowledge of European and American legislation on clinical trial design, structure and content of essential documents


  • We are interested in finding full-time staff. Remote medical writers and freelancers are also welcome!
  • Salary is to be determined based on results of the interview

All Careers

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