ICU Clinical Research Coordinator - Pulmonary/Critical Care

University of California - San Diego Medical Centers; San Diego (CA); On-site; USD 76,000 - 122,000; Full time

Job summary

UC San Diego Health is seeking an Assistant Clinical Research Coordinator in the Pulmonary, Critical Care & Sleep Medicine Division to support IRB submissions, protocol management, data collection, and regulatory tasks for ICU recovery studies.

Under supervision, you will screen patients, coordinate study startup, recruit participants, manage files, and assist with analyses and reporting, while ensuring compliance with FDA, NIH, GCP and HRPP requirements.

Qualifications

• Bachelor's degree or equivalent combination of education and experience.
• Experience performing clinical research duties in a clinical research environment.
• Demonstrated experience interpreting medical charts and abstracting data from records.
• Experience coordinating study startup activities and regulatory submissions.
• Knowledge of FDA policies regulating clinical trials and HRPP requirements.

Responsibilities

• Coordinate and manage clinical trials, including patient eligibility screening, data collection and analysis, and protocol compliance.
• Process IRB submissions and amendments; assist regulatory submissions and safety reports.
• Communicate with physicians and disease groups; schedule and recruit participants; maintain clinical research files.
• Assist with data preparation, data extraction, and statistical analyses; support onboarding of staff and volunteers.

Skills

Clinical research experience

IRB submissions

Data abstraction/data entry

Regulatory knowledge (FDA/NIH/GCP)

Communication skills

Team coordination

Education

Bachelor's degree or equivalent experience

Tools

Velos

Access

Excel

MS Word

Job description

UC San Diego Health is seeking an Assistant Clinical Research Coordinator in the Pulmonary, Critical Care & Sleep Medicine Division to support IRB submissions, protocol management, data collection, and regulatory tasks for ICU recovery studies.

Under supervision, you will screen patients, coordinate study startup, recruit participants, manage files, and assist with analyses and reporting, while ensuring compliance with FDA, NIH, GCP and HRPP requirements.