Medical writer

Contract, full-time
3+ years

What should be done?

  • Writing documentation for research of routine clinical practice (synopsis; research protocol; informed consent; instructions and guidelines for investigators);
  • Writing final reports on the results of studies of routine clinical practice, statistical reports on the results of statistical analysis;
  • Preparation of literary reviews, scientific reports, reports, publications;
  • Verification of documentation for compliance with the requirements of the regulatory authorities of the Russian Federation and with the requirements of customers;
  • Quality control, editing and correction of errors in design documentation;
  • Interaction with the project team during the development of documentation.

Expectations from the candidate

  • Higher medical / pharmaceutical education;
  • More than 3 years of experience in writing documentation for clinical trials: protocols, investigator brochures, research reports;
  • Knowledge of legislative and regulatory legal acts, methodological materials and rules governing clinical trials;
  • Knowledge of the provisions of Good Clinical Practice (ICH GCP);
  • Knowledge of English (at least Upper-Intermediate);
  • Confident PC user, knowledge of text and graphic editors for working with text and images;
  • Analytical mindset, organizational skills, responsibility, the ability to prioritize, completing tasks on time.

What do we offer?

  • Join the most promising project in the field of medical data in the country and in the world - creating a world leader in research of routine clinical practice with subsequent integration with genetic data;
  • It is possible to register under the Labor Code of the Russian Federation with full employment, we also consider part-time employment, remote work - registration of an individual entrepreneur, self-employed;
  • Salary is discussed individually with the candidate.
  • Opportunity for professional growth in a dynamically developing company.
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