Medical Writer vacancy

Location:
Moscow or St. Petersburg, Russia
Reports to:
Director of Scientific Department
Duties and Responsibilities:
This position will be responsible for clinical study documents preparation:
  • Protocol
  • Investigator's Brochure
  • ICF
  • Clinical Study Report
Education Requirements:
MD, PhD
Experience:
Minimum of 2 years experience in clinical trials.
About Smooth Drug Development
Smooth Drug Development is a full-service CRO operating in Russia and CIS and providing a wide spectrum of clinical trials services.