Clinical Research Associate

SYREON CORPORATION is a dynamic contract research organization conducting comprehensive phase I-IV clinical research via advanced digital technologies in over 40 countries. Syreon partners with a select portfolio of international pharmaceutical 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 a Clinical Research Associate in Canada to join its Clinical Project Management Division. The CRA, with direction and supervision from the Trial Project Manager and Director of Operations, is responsible for the investigative site management in accordance with Syreon’ s SOP’s, Working Practices, GCP/ICH Guidelines and regulatory requirements.

Responsibilities include:

• RA/IRB submissions
• Site visits and training
• General site support
• Regulatory documentation and reports
• Data verification
• CRA oversight and co-monitoring

Desired Skills and Experience:

Applicants should have a minimum of five 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.

If you like to be challenged and prefer working with a team committed to excellence then we would like to hear from you.

For more information about Syreon please visit our website: www.syreon.com

Only candidates selected for an interview will be contacted.