Assistant Clinical Research Coordinator: Data, Consent & Trials

Stanford University; Palo Alto (CA); On-site; USD 39,950 - 46,838; Full time

Job summary

Stanford University is seeking an Assistant Clinical Research Coordinator to provide administrative support for clinical data collection and study coordination. You will work under the supervision of the principal investigator and study coordinators, handling regulatory documents, consent forms, and scheduling calls with participants.

The role includes screening and consenting participants, administering questionnaires, collecting data, performing basic measurements under protocol, and assisting

Qualifications

• Two-year college degree and one year of relevant experience or an equivalent combination of experience, education, and training.
• General knowledge of medical terminology.
• Working toward certification to perform basic patient measurements and tests (phlebotomy, EKG).

Responsibilities

• Schedule and call subjects for appointments and reminders.
• Prepare, distribute, and process questionnaires.
• Maintain regulatory documents, consent forms, and logs.
• Assist with screening, recruitment, and obtaining consent of study participants.
• Administer questionnaires and tests; code data for entry; review forms for completeness.
• Extract data from source documents and complete case report forms.
• Perform basic measurements and tests (vital signs, phlebotomy, EKG) under protocol.
• Prepare, process, and ship specimens; order equipment and supplies.
• Process study compensation payments and thank-you letters; assist with post-study activities.
• Other duties may be assigned.

Skills

General knowledge of medical Termin..

Certification pursuit (phlebotomy/EKG)

Education

Two-year college degree with 1 year experience

Job description

Stanford University is seeking an Assistant Clinical Research Coordinator to provide administrative support for clinical data collection and study coordination. You will work under the supervision of the principal investigator and study coordinators, handling regulatory documents, consent forms, and scheduling calls with participants.

The role includes screening and consenting participants, administering questionnaires, collecting data, performing basic measurements under protocol, and assisting