Assistant Clinical Research Coordinator

Stanford University School of Medicine is seeking an Assistant Clinical Research Coordinator to provide administrative support and coordination of clinical studies within the CDAC Lab. This role operates under the supervision of the Principal Investigator and supports day\-to\-day study operations in accordance with institutional and regulatory guidelines. This is a hybrid position requiring both on\-site and remote work. Employees are expected to work on\-site several days per week, subject to operational needs. **DESIRED QUALIFICATIONS:** Bachelor’s degree in the sciences preferred. **PHYSICAL REQUIREMENTS\*:** * Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping. * Occasionally sit, reach above shoulders, perform desk\-based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds. * Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more. *\* \- Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.* **WORKING CONDITIONS:** May require extended or unusual work hours based on research requirements and business needs. * **WORK STANDARDS:** * Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations. * Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned. * Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide, http://adminguide.stanford.edu . **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,