Clinical Trials Coordinator

St. Petersburg,Moscow
3 years
Contract, full-time

The Clinical Trials Coordinator (CTC) coordinates the work of CRAs and provides assistance to the Project Manager in clinical trials conduct.

Responsibilities:

  • To communicate with sponsors concerning non-medical study issues
  • To assist in the organizing and holding of study related meetings/training
  • To assist in the preparation and reporting of project statuses
  • To control investigator invoices
  • To assist in managing Investigators' Meetings
  • To assist in the coordination of the activity of all departments and units involved in the project
  • To assist in the creation of study specific procedures, the preparation of investigator files, and the maintenance of TMF
  • To translate study documents
  • To assist in regulatory package preparation and submission
  • To assist in the preparation of financial reports, and others.

Requirements: 

  • Higher education (Philology or Linguistics preferred)
  • Excellent English and Russian (spoken and written)
  • Ability to work under demanding time schedules
  • Strong leadership and ability to learn
  • Presentation skills 

Conditions:

  • We are based in Saint Petersburg and Moscow and are interested in finding full-time employees
  • Salary is to be determined based on results of the interview

All Careers

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If you have not found what you have been looking for, send a request to info@oct-clinicaltrials.com.

Get in Touch with OCT Clinical