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 Russian, 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
Thank you for your request! Our team will respond to you within 24 hours.
We've merged with Palleos Healthcare GmbH to form a wide-reaching European CRO
OCT Clinical is now operating under Palleos Healthcare brand name.
“The merger will undoubtedly create significant synergies, not just doubling but squaring the expertise of both companies”, Philip Räth, Ph.D., managing director at Palleos, said in the release.
“OCT Clinical is proud to join forces with palleos healthcare, as it has an excellent reputation in the industry it serves. Now we can offer tailored solutions to our clients to meet their diverse clinical research needs and accelerate the time of bringing their products to market”, Dmitry Sharov, CEO at OCT Clinical.
