We are looking for a highly qualified candidate for a position of a full-time and part-time clinical trial monitor in Russia, Ukraine, Belarus, Bulgaria, Latvia, Lithuania, and Estonia. This position presumes primarily responsibilities of monitoring (pre-study, initiation, routine, and close-out visits) of investigator sites for the compliance to the study protocol, ICH GCP, client SOPs and applicable local regulations. Up to 50% travel is anticipated. The responsibilities will also include recruit investigators for participation in the clinical trails, negotiate study budgets, obtain, review for appropriateness, and process regulatory and administrative documents from the investigator sites.
At least, medical degree (MD) or PhD degree in life science is required. Experience as a CRA, Principal Investigator, Sub-Investigator or Study Coordinator for at least one year is a must. The candidate should be highly motivated, responsible, willing to travel on an as needed basis and have advanced level of written and spoken English.
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