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 a RN may be considered. Prefer scientific discipline and multiple therapeutic experiences. 1 year 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. Bilingual in French/English a requirement.
What we Offer:
Advanced Group is proud to be an Equal Opportunity Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, disability, sexual orientation, ancestry, marital or veteran status.
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