Clinical Research Associate I - Russia

Global CRO company is looking to recruit Clinical Research Associate I (CRA I) for their office in Novosibirsk (Russia) to identify, select, initiate and close-out appropriate investigational sites for clinical studies. To monitor those sites in order to ensure that studies are carried out according to the study protocol and in accordance with company SOPs/WPs, applicable regulations and the principles of ICH -GCP

Responsibilities:

• Familiarity with Clinical Research SOPs/WPs, ICH-GCP and appropriate regulations.
• Familiarity with principles of investigator recruitment.
• Co-ordinate all the necessary activities required to set up and monitor a study.
• Design patient information sheets and consent forms.
• Coordinate documents translation, verification and back translations where required.

QUALIFICATIONS/EXPERIENCE REQUIRED:

• Medical/science background and relevant experience.
• Ability to review and evaluate clinical data.

If you have the relevant experience please send your updated C.V. to janka@clinicalprofessionals.co.uk.

Keywords: CRA I Clinical Research Associate I Russia Novosibirsk office-based Monitor of clinical research

QUALIFICATIONS/EXPERIENCE REQUIRED:

• Medical/science background and relevant experience.
• Ability to review and evaluate clinical data.