Clinical Research Associate (CRA) Jobs

Lake Forest, IL

Responsibilities

Responsibilities primarily involve management of assigned investigational study sites including: prestudy, initiation, monitoring and study close-out site visits. Approximately 65% travel overall can be expected. In line with ICONâ??s philosophy of providing the highest quality to our clients, CRAs are typically assigned to one to two programs at a time and participate in continuous training.

 Qualifications

Applicants should possess a Bachelor's degree in the life sciences or nursing or an equivalent combination of education and work experience. Applicants must have at least **12 months of experience monitoring pharmaceutical clinical trials. Excellent communication and organizational skills are essential. An ICON CRA must be able to travel overnight, primarily in the USA, 3 days per week on average.

 Equal Employment Opportunity

 ICON Clinical Research is an Equal Opportunity Employer committed to strength in diversity.

For information please email info@iconus.com