Clinical Research Associates, All locations

The drive to succeed. It never ends.Broad and dynamic challenges that develop new skills. Working with a company that does more than evolve…it sets standards. These are your career goals. ICON Clinical Research is your company.At ICON Clinical Research, we see and do things differently. Dedicated to providing the pharmaceutical and biotechnology industries with exceptional clinical research and biometrics services, we're the first CRO to be awarded ISO 9002 quality certification across all functions. Join us and build a remarkable career... one that will set a new criterion for success.
Clinical Research Associates
All locationsResponsibilities will primarily involve management of assigned investigational study sites including: prestudy, initiation, monitoring and study close-out site visits. Approximately 60% travel overall can be expected. In line with our philosophy of providing the highest quality to our clients, CRAs are only assigned to one program at any one time and participate in continuous training.Home-based CRAs will be considered.Applicants should possess a B.S. degree in the life sciences or nursing and have at least 2 years of experience monitoring pharmaceutical clinical trials. We are seeking candidates with experience in the following therapeutic areas: Oncology; Diabetes; Pediatrics (any indications); Anti-Infective; and Inpatient Monitoring Experience. Excellent communication and organizational skills are essential.
Job Requirements
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