Clinical Research Support Specialist

Stanford Reglab; California; On-site; USD 40,000 - 65,000; Full time

Job summary

Stanford University is seeking an Assistant Clinical Research Coordinator to provide administrative support for the collection of clinical data and coordination of clinical studies. You will work under supervision of the principal investigator and study coordinator.

The role involves scheduling, screening, consent processes, data entry, and regulatory documentation to ensure study quality and compliance. Candidates should have a two-year degree and relevant experience, with progress toward

Qualifications

• Two-year college degree with one year of relevant experience or equivalent combination.
• Working toward certification to perform basic patient measurements and tests such as phlebotomy and EKG.
• Must possess California driver license if applicable.

Responsibilities

• Schedule and/or call subjects for appointments; contact participants with reminders or other requirements.
• Prepare, distribute, and process questionnaires.
• Maintain regulatory documents and consent forms; file correspondence.
• Assist with screening, recruiting, and obtaining consent of study participants.
• Review medical records and conduct interviews to gather data.
• Code data for computer entry; perform basic measurements and tests per protocol after training.
• Prepare, process, and ship specimens/samples according to requirements.
• Order and maintain equipment and supplies.
• Process study compensation payments and thank you letters to subjects.

Skills

General knowledge of medical terminol

Education

Two-year college degree and one year of relevant experience

Job description

Stanford University is seeking an Assistant Clinical Research Coordinator to provide administrative support for the collection of clinical data and coordination of clinical studies. You will work under supervision of the principal investigator and study coordinator.

The role involves scheduling, screening, consent processes, data entry, and regulatory documentation to ensure study quality and compliance. Candidates should have a two-year degree and relevant experience, with progress toward