Selection of potential centres and carrying out assessment visits to participate in research;
Preparation and filing of study documents, for approval by the regulatory authorities;
Monitoring studies in accordance with the rules of GCP and clients’ SOPs;
Reporting on project status;
Provide study file support and monitoring of quality maintenance and storage of documentation in study centers.
Graduate medical education (possibly pharmaceutical);
Desirable experience as a physician, pharmacist, Сlinical Trial Assistant or co-investigator;
Knowledge of English (Intermediate level and above);
Knowledge of GCP standards.
Salary according to interview results;
Additional benefits (paid meals, transportation and voluntary medical insurance; compensation for mobile phone and internet bills).