Clinical Research Coordinator: Trials & Protocol Support

UC San Diego Health; San Diego (CA); On-site; USD 76,000 - 122,000; Full time

Job summary

UC San Diego Health's Department of Medicine seeks a Clinical Research Coordinator to coordinate and manage clinical trials, including screening for eligibility, data collection, and protocol adherence, under the supervision of the Clinical Research Supervisor.

The role supports regulatory submissions, liaison with investigators and IRB, and ensures accurate research files and timely reporting of adverse events.

Qualifications

• Bachelor's degree or equivalent education/experience.
• Experience performing clinical research duties in a clinical environment.
• Experience with laboratory procedures and interpreting results.
• Experience with FDA policies regulating clinical trials.
• Experience completing case report forms.

Responsibilities

• Coordinate and manage clinical trials, including protocol management and screening for eligibility.
• Data collection, entry, and analysis; monitor patient treatment and adverse events.
• Maintain accurate clinical research files and VELOS study records.
• Assist with regulatory submissions, renewals, and safety reports.
• Liaise with Investigators, IRB, and study sponsors; support account statements and invoicing.

Skills

Clinical research coordination

Data collection

Regulatory understanding

IRB communication

Team collaboration

Education

Bachelor's degree

Tools

Velos

Excel

MS Word

Access

Job description

UC San Diego Health's Department of Medicine seeks a Clinical Research Coordinator to coordinate and manage clinical trials, including screening for eligibility, data collection, and protocol adherence, under the supervision of the Clinical Research Supervisor.

The role supports regulatory submissions, liaison with investigators and IRB, and ensures accurate research files and timely reporting of adverse events.