Assistant Clinical Research Coordinator

Clinical Research Coordinators (CRCs) support, conduct, coordinate or manage the clinical research studies or trials on human subjects. Principal and co-investigators provide the overall direction in a clinical study, but CRCs can have significant roles in clinical study activities.

Stanford University is seeking an Assistant Clinical Research Coordinator to p erform administrative support duties related to the collection of clinical data and/or the coordination of clinical studies. Work under supervision of the principal investigator and/or study coordinator/supervisor.

Qualifications

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• APPLICABLE. REMOVE IF NOT APPLICABLE]
• Drivers License Requirements
• Must possess and maintain a valid California non-commercial Class
• C Driver's License.
• Ability to drive day or night.
• When conducting university business, must comply with the California Vehicle Code and Stanford University driving requirements.

Responsibilities

• Core Duties: Schedule and/or call subjects for appointments; contact participants with reminders or other requirements.
• Prepare, distribute, and process questionnaires.
• Perform clerical duties in the preparation of regulatory documents. Maintain all forms and documents, including consent forms and master subject logs. File all appropriate correspondence.
• Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews to gather data, as needed.
• Administer standard study questionnaires and tests, score test measurements and questionnaires, and code data for computer entry. Perform quantitative review of forms, tests, and other measurements for completeness and accuracy.
• Extract data from source documents for research studies as directed. Collect data and complete case report forms.
• Perform basic measurements and tests on patients according to protocol, such as obtaining vital signs and performing phlebotomy and EKG, after appropriate training/certification. Collect study specimens according to protocol.
• Prepare, process, and ship specimens/samples accurately under well-defined requirements.
• Order and maintain equipment and supplies.
• Process study compensation payments and thank you letters to subjects upon completion of trial activities. Assist with post-study activities, as needed.
• Minimum Education and Experience
• Two-year college degree and one year of relevant experience or an equivalent combination of experience, education, and training.
• Knowledge, Skills and Abilities: General knowledge of medical terminology.
• Certificates and Licenses Required
• Working toward certification(s) to perform basic patient measurements and tests, such as phlebotomy and EKG.
• Must possess and maintain a valid California non-commercial Class C Driver's License, if applicable.