Assistant Clinical Research Coordinator

Job Purpose:
Perform administrative support duties related to the collection of clinical data and/or the coordination of clinical studies. Work under the close direction and supervision of the principal investigator and/or study coordinator/supervisor.

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.

Requirements: Minimum Requirements:
Education & 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.

Certifications and Licenses:
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.

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.
Ability to drive day or night, if applicable.
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 the job.

Title: Assistant Clinical Research Coordinator (ACRC)
Location Address: 800 Welch Road, Palo Alto
Remote/onsite/hybrid:  Hybrid and onsite 4 days per week during training
Duration of project (start and end date): approximately 6 months
Full time or part time: Full time
Number of hours per week: 40
Shift timing/schedule: Day
Will the resource be working with minors No
How many years of experience are required  1
Will this role extend or possibly convert to a Stanford FTE That is the plan
Top 3 requirements to hire  Assistant research experience, prefer oncology and treatment trials, as well as EPIC knowledge
Questions that determine what background check package to run Is a degree required for this job (this will alert Magnit that an education check is needed) No, but highly preferred since they cant be promoted without a degree
Is driving required for this job (this will alert Magnit that a MVR is needed) No.