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Clinical Research Associate Warsaw Poland,  

Posted on : 08 March 2017

Project Description

  Location: Poland and other KCR locations (office-based or home-based)   The duties associated with the role include:   Performing site visits and monitoring activities in accordance with protocol, GCP/ICH Guidelines and other applicable requirements Ensuring overall integrity of study and adherence to guidelines, protocol and regulations Taking an active role in the project team by providing feedback and suggestions for successful completion of the project Coaching and mentoring less experienced CRAs to assist in their development and training Requirements:   University degree in life sciences/pharmacy/biotechnology At least 1 year of independent monitoring experience (including pre-study, initiation, routine monitoring and close-out visits) according to protocol monitoring guidelines, SOPs, GCP/ICH Guidelines Computer competency Fluent command of English Ability to complete tasks in an accurate and timely manner If you wish to apply, please submit your CV using the button below.  


Poland Warsaw

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