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Clinical Research Associate (CRA)

Accell Clinical Research is looking for a determined and motivated Clinical Research Associate (CRA) ready to work in St. Petersburg Clinical Headquarters and to travel across Russia, CIS, and Eastern Europe, as well as for local CRAs within Eastern Europe and CIS.

CRA is responsible for monitoring performance of all study sites from A to Z and providing a link between a project team and investigators. CRA’s primary focus is expected to be on meticulous site management via executing all types of site visits, monitoring sites’ deliverables, IMP, and all related items supply. Other responsibilities include, but are not limited, to:

– insurance of the project’s high quality and protocol adherence;

– timely and accurate reporting and documentation maintenance (including preparation and update of all study reports);

– site selection (in a close collaboration with the study project manager);

– site performance evaluation and site metrics report.

We are looking for a professional with a solid knowledge of written and spoken English (upper-intermediate level or higher), university degree in the health-related field (Medical Doctor degree would be a plus), strong work ethics and sound management skills, and at least 1 year of clinical research work experience. The person applying should be willing to actively participate in the corporate life of the company (including training sessions and other activities) and to travel a lot (approximately 50% of the total working time).

If you believe you have what it takes to become a part of Accell’s team, click ‘Apply Now’ button, fill out the pop-up form and send it to us.

Updated on: July 10, 2018.

This position is available in the following countries:
Russia
Ukraine
Serbia
Bulgaria
Romania
Georgia
Lithuania
Slovakia

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