Senior Clinical Research Associate

Duties: The Sr. CRA is responsible for administering clinical trial activities. This position assists with performing in-house study management responsibilities, traveling to clinical sites to perform monitoring and site management responsibilities, ensuring site performance and adherence to the protocol, company procedures, local, state, GCP/ICH, FDA, and other required regulations and guidelines. Responsibilities include clinical site management, collecting and tracking study documentation, tracking study costs, and development of study-related documents. Requirements: Bachelor's degree preferably in the Life Sciences or health-related field and a minimum 3-4 years as a study monitor (depending on education/related experience) plus experience assisting with in-house study management in a clinical research environment Knowledge of ISO 13485:2003, US FDA QSR, ICH and other system requirements relating to the Medical Device Industry. Must be a team player, have strong communication skills, organization skills, strong computer literacy and the ability to travel 30% of the time.

To find out more about Real please visit www.realstaffing.com [1]

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[1] http://www.realstaffing.com