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- Provides support in proper research protocol compliance and development, including regulatory controls, study procedures, and data management.
- Assists in preparation and maintenance of study and subject level documentation, reports, and other materials; keeping appropriate logs; tracking participants; and preparing study materials.
- Under direct supervision, performs a variety of tasks: assists in recruitment and screening of prospective research participants; obtains informed consent from study participants for minimal risk studies (as needed); collects, enters, and analyzes subject data; and compiles reports.
- Reviews new protocols for biological specimen requirements; assures all necessary supplies are on site; prepares and/or oversees the preparation of biological specimens for shipment to reference laboratory.
- Assists in preparation for site initiation, monitoring, and audit visits.
- Assists in orientation of new clinical research staff.
Clinical Research Specialist - Greensboro, United States - Cone Health
Description
Overview:
EDUCATION: Required: High School Diploma or equivalent
Preferred: Bachelor's Degree or higher EXPERIENCE: Required: One year experience in clinical research or relevant area. LICENSURE/CERTIFICATION/REGISTRY/LISTING: REQUIRED: Obtain Good Clinical Practice certification within 30 days of hire and maintain without lapse.
Obtain Human Subjects Research certification within 30 days of hire and maintain without lapse.
PREFERRED