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.