Clinical Research Coordinator

As a Clinical Research Coordinator within our team, you will be overseeing coordinating our procedural tasks and documentation for our clinical trials running on-site.

Our mission within this group is to bring clinical research to as many lives as possible, while delivering unparalleled service and exceptional value to our clinical trial partners and your responsibilities will included but aren't limited to the following.

• Participate in the early planning phases of clinical study by providing assistance in the preparation of study proposal timelines, scheduling and other study requirements as appropriate
• Evaluate, coordinate, and ensure the completion of all protocol related tasks
• Coordinate with Study or Project Manger to ensure appropriate timelines are being met as per contractual obligations
• Participate in meetings to include (pre-planning and clinical tracking).
• Coordinates with Screening and Recruitment to maintain timely execution of study enrolment

Role Requirements:

• Bachelor's Degree in medicine, science or equivalent degree would be desirable but not essential
• Excellent communication, planning and decision-making skills
• Must be able to utilize computer-based applications such as Microsoft Office and other web based systems including CTMS systems

Benefits of Working in ICON:

ICON provides you with the innovative resources to be successful in delivering results, inspiring others and becoming a trusted partner. We offer an exceptional benefits package that includes a comprehensive health plan, retirement plans, highly competitive pay, corporate bonus plan, time away from work, and many other incentives amongst an opportunity to grow your career within ICON.

What's Next?

Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.*LI

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