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Clinical Research Assistant


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Clinical Research Assistant needs BS/BA, MS is desirable 5+ years of site management of which a minimum of 2 years field monitoring experience

Clinical Research Assistant requires;

IVD Stud Experience
Medidata RAVE system
applicable standards and regulations for clinical trial
Cardiovascular Therapeutic area

Clinical Research Assistant duties:

Oversight of monitoring visit scheduling, site and monitoring performance metrics, issue escalation and corrective actions.
Development of training materials and study tools for site and CRA use
Assistance in formation of the Adjudication Committee including oversight of documentation collection and filing into the Trial Master File

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Denise Farris, Clinical Research Coordinator

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