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.
Requirements:
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
Conditions:
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
