The Stanford Center for Clinical Research (SCCR), in collaboration with the Stanford Departments of Medicine, Neurosurgery, Bioengineering and Radiology, is conducting longitudinal studies. SCCR is seeking to hire multiple Clinical Research Assistants to support enrolling athletes at Stanford and other study sites in the Bay Area.

SCCR provides infrastructure and research support to Stanford clinical research investigators. Its mission is to conduct and promote high-impact, innovative clinical research to improve human health.

The Clinical Research Assistant will work within a multidisciplinary team, including physicians, athletic trainers, coaches and Clinical Research Operations Specialist; and have direct interaction with participants. The Clinical Research Assistant is required to have the ability to multi-task in a high-energy environment. This position involves traveling to study sites and being able to attend athletic games and practice sessions. The Clinical Research Assistant is required to have flexibility in their work schedule, and outstanding communication and organizational skills--with attention to detail. The study visits may occur in the evenings and occasionally during weekends. The Clinical Research Assistant will be responsible for ensuring compliance with federal, state, local, and sponsor regulations and work under the direction of their supervisor.

At SCCR, we strive to find team members who are passionate about their work, flexible, fun, and want to deliver results. We place a high priority on equipping our staff to perform their job efficiently, helping them acquire new skills and grow within the organization. We encourage our team to have a healthy balance between work commitments and life outside of work, and provide support to achieve this balance. If you are looking to make a large impact through global-reaching clinical research, we encourage you to apply!

Duties include:

• 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.
• 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.

*- The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned.