I’m looking for a Medical Writer based anywhere in Europe to work closely with the Senior Medical Writers and under the supervision of the Head of Medical Affairs Unit at a small-midsized CRO.
This medical writer will be responsible for drafting, editing and reviewing preclinical/clinical documents such as preclinical and clinical study reports, study protocols, patient information and informed consent forms as well as other medical and regulatory documents (including Investigators’ Brochure, IMPD, Briefing Document for Scientific Advice and follow-up scientific advice, CTD).
Fluent in English
Master’s degree in biomedical/scientific disciplines
At least 1.5 years of working experience in clinical research or pre-clinical research
Knowledge of medical concepts and terminology
If you are interested in discussing this role in further detail, please don’t hesitate to reach out to me: firstname.lastname@example.org / +441273 952187
Salary: On application
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