A Clinical Research Associate (CRA) is responsible for conducting monitoring activities at a clinical site(s) for a clinical trial(s).The CRA may be responsible for multiple projects and must be able to work both independently and in a team environment.
The ideal candidate should have a Bachelor’s degree but an RN may be considered. Prefer scientific discipline and multiple therapeutic experiences. Three (3) or more years of monitoring experience in oncology or combination of on-site monitoring and clinical research experience or education; industry certification preferred. The ability to perform national travel up to an average of 80%, depending on project needs. The candidate must have excellent verbal and written communications skills; excellent interpersonal and organizational skills with demonstrated attention to detail. The candidate must be computer literate with proficiency in MS Office including Word, Excel, and PowerPoint.
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