Contract Clinical Research Associate

SYREON CORPORATION is a dynamic contract research organization conducting comprehensive phase I-IV clinical research via advanced digital technologies in over 30 countries. Syreon partners with a select portfolio of international biopharmaceutical clients to identify therapeutic trends, streamline new drug evaluation, monitor clinical use and economics, and control development costs and investment risk by accelerating time to market.

Syreon Corporation is currently seeking contract monitors across all regions throughout the United States.

Responsibilities consist of performance of on-site monitoring duties, including source document verification, conduct of site initiation visits, routine monitoring visits and close-out visits to ensure the integrity of the clinical data, adherence to Good Clinical Practice and the study protocol.

Applicants should have a minimum of two years experience in clinical trial monitoring. Formal Good Clinical Practice training and a B.Sc. or RN (or related) degree is also required. Excellent interpersonal and professional skills are mandatory. Fluency in French preferred for eastern Canada monitors.

For more information or to apply please visit the careers page of our website at http://www.syreon.com/admin/careers.asp

Only candidates selected for interview will be contacted.