Russia - Moscow, St. Petersburg, Novosibirsk


CRA

MB Quest is seeking experienced clinical research associates to monitor and manage domestic and international trials. These are full-time office based positions in Moscow, St. Petersburg, and Novosibirsk.

Key Responsibilities:

  • Manage activities associated with studies
  • Create and review informed consent, study reports and monitoring tools
  • Organize and conduct investigator meetings
  • Research and resolve data queries
  • Interact with senior staff regarding objectives and status of clinical projects
  • Prepare reports and make presentations
  • Ensure regulatory compliance with ICH/GCP guidelines, and company SOP’s

Requirements:

  • Minimum of 1 year of clinical trial monitoring experience as a CRA
  • Fluent in written and spoken English
  • MD preferred
  • Thorough knowledge of ICH/GCP guidelines

For confidential consideration, please send CV and salary requirements to hr-russia@mbquest.net.
Compensation will be based on experience.

PRINCIPALS ONLY .

NO PHONE CALLS PLEASE.