Job description

Duties: Coordinate clinical research studies; assist with subject recruitment and consent; conduct patient interviews using standardized scales; supervise collection of study laboratory samples, assist with collecting, organizing and entering data into established database files; maintain research records, subject contact logs, data files and prepare study-related reports; liaison with clinicians, research pharmacist, sponsor and institutional review boards.

Qualifications: BA/BS degree, preferably in psychology, pharmacology, social or biological sciences, and 1 to 3 years of experience in a clinical, clinical trial or research setting, or an equivalent combination of education and experience, are required. Knowledge of IRB and human research protection regulations required; attention to detail and accuracy in data collection and quality assurance required; good organizational and interpersonal skills; must be able to work independently and balance several tasks effectively; experienced with computer-based recording and basic operations. Position contingent upon continued funding.

Reference Number: 40-27195

Salary Grade: 025

Employment Type: Exempt

Org: PS-Addictions

Special Requirements: Background check required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.

Job Family: I-Technical/Professional Research




Diversity Profile: University



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Job No:
Posted: 11/4/2017
Application Due: 5/11/2018
Work Type: