Neuroimaging Clinical Research Coordinator

University of California, San Francisco; San Francisco (CA); On-site; USD 65,000 - 90,000; Full time

Job summary

University of California, San Francisco seeks a Clinical Research Coordinator to join its brain imaging groups within the Department of Radiology and Biomedical Imaging. You will coordinate research protocols, manage data, and enroll participants under PI oversight in a fast-paced environment.

Responsibilities include ensuring regulatory compliance, maintaining study data integrity, and supporting audits while training staff and coordinating cross-department workflows.

Qualifications

• High School Diploma or equivalent experience.
• Excellent organizational and communication skills, with attention to detail.
• Ability to work independently and manage multiple projects with deadlines.
• Experience coordinating clinical research imaging studies is preferred.

Responsibilities

• Coordinate research brain imaging studies under supervision and PI oversight.
• Manage data collection, databases, and comprehensive datasets for multiple studies.
• Enroll and consent patients into research protocols and ensure compliant documentation.
• Maintain regulatory documents and oversee IRB submissions, renewals, and amendments.
• Assist with staff training, audits, and quality control procedures.
• Interface with departments to obtain approvals and ensure patient safety and confidentiality.

Skills

Organizational skills

Multi-tasking

Attention to detail

Verbal and written communication

Independent work

Patient interaction

Time management

Education

Bachelor's or higher in neuroscience, biology, biomedical imaging, applied math, engineering, or related field

Tools

Matlab

Python

SPSS

R

Stata

Access

Job description

University of California, San Francisco seeks a Clinical Research Coordinator to join its brain imaging groups within the Department of Radiology and Biomedical Imaging. You will coordinate research protocols, manage data, and enroll participants under PI oversight in a fast-paced environment.

Responsibilities include ensuring regulatory compliance, maintaining study data integrity, and supporting audits while training staff and coordinating cross-department workflows.