Dermatology Clinical Research Coordinator — Study Data

Stanford University; Palo Alto (CA); On-site; USD 55,000 - 75,000; Full time

Job summary

Stanford University’s Department of Dermatology seeks an Assistant Clinical Research Coordinator to provide administrative support for clinical data collection and the coordination of studies.

The ACRC will assist with both federally funded and non-federal research, under the supervision of the principal investigator and the clinical research manager, with in-person work at the Redwood City and Palo Alto sites.

Qualifications

• Bachelor’s degree in medicine or scientific field required.
• Proven ability to work independently and take ownership of a project.
• Proven ability to work collaboratively and cooperatively in a team environment.
• Ability to balance multiple projects and timelines.
• Strong oral and written communication skills.
• Detail-oriented with excellent organizational skills.

Responsibilities

• Schedule and coordinate subject appointments and reminders.
• Prepare, distribute, and process questionnaires.
• Assist with the preparation of regulatory documents and maintain logs.
• Screen, recruit, and obtain consent of study participants.
• Review medical records and conduct interviews to gather data.
• Administer study questionnaires and code data for entry.
• Extract data from source documents and complete case report forms.
• Perform basic measurements and tests as directed.
• Prepare, process, and ship specimens.
• Order and maintain equipment and supplies.

Skills

Independent work

Team collaboration

Multi-tasking

Communication skills

Attention to detail

Computer literacy including AI tools

Education

Bachelor’s degree in medicine or scientific field

Job description

Stanford University’s Department of Dermatology seeks an Assistant Clinical Research Coordinator to provide administrative support for clinical data collection and the coordination of studies.

The ACRC will assist with both federally funded and non-federal research, under the supervision of the principal investigator and the clinical research manager, with in-person work at the Redwood City and Palo Alto sites.