Clinical Research Coordinator - Pediatric Behavioral Studies

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

Job summary

UC San Diego Health Center for Healthy Eating and Activity Research in the Department of Pediatrics seeks a contract/limited-position research coordinator to screen for eligibility, collect data, ensure protocol compliance, monitor treatment, and maintain accurate clinical files. You will work under supervision and interact with PIs and project staff.

The role involves regulatory support, attendance at weekly meetings, and completing required trainings, with evening shifts up to three nights per

Qualifications

• Theoretical knowledge of social sciences, psychology, clinical sciences, nutrition, or public health.
• Experience performing clinical research duties in a clinical research environment.
• Experience using database, word processing and spreadsheet applications (Velos, Access, Excel, MS Word).
• Experience providing in-service training to research personnel on protocols and procedures.
• Excellent planning and organizational skills in a high-volume, deadline-driven setting.
• Excellent interpersonal and written/verbal communication skills, including professional phone etiquette.

Responsibilities

• Screen for participant eligibility, collect data, ensure protocol compliance, monitor treatment, and maintain clinical research files.
• Assist regulatory with Human Subjects safety reports.
• Communicate with principal investigators, COIs, project directors, and other staff; attend weekly meetings and trainings.
• Perform other duties as assigned.

Skills

Clinical research experience

Statistics software

Data management

Communication skills

Confidentiality

Job description

UC San Diego Health Center for Healthy Eating and Activity Research in the Department of Pediatrics seeks a contract/limited-position research coordinator to screen for eligibility, collect data, ensure protocol compliance, monitor treatment, and maintain accurate clinical files. You will work under supervision and interact with PIs and project staff.

The role involves regulatory support, attendance at weekly meetings, and completing required trainings, with evening shifts up to three nights per