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.
- 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
- 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 email@example.com.
Compensation will be based on experience.
PRINCIPALS ONLY .
NO PHONE CALLS PLEASE.