Pediatric Clinical Research Coordinator — Study Operations Pro

University of California - San Francisco; San Francisco (CA); On-site; USD 70,000 - 90,000; Full time

Job summary

University of California - San Francisco is seeking a Clinical Research Coordinator to execute, manage, and coordinate pediatric research protocols under supervision. The role involves coordinating data collection, regulatory compliance, and study logistics across several concurrent studies.

The CRC will oversee data integrity, IRB submissions, staff training, and collaboration with physicians and study teams to ensure timely and accurate study progress while adhering to regulatory standards.

Qualifications

• Experience coordinating clinical research studies and data collection.
• Familiarity with IRB processes, protocol submissions, and study documentation.
• Knowledge of regulatory standards and patient safety requirements.

Responsibilities

• Identify subjects, screen and enroll, and coordinate study visits.
• Manage data entry, databases, and data quality across studies.
• Coordinate staff schedules and oversight of protocol adherence.
• Maintain regulatory documents and assist with IRB submissions.
• Communicate with investigators, departments and external teams.

Skills

Coordination

Data collection

IRB processes

Regulatory compliance

Patient interaction

Education

BA/BS in life sciences

Tools

IRB online system

Database management

SQL / queries

Job description

University of California - San Francisco is seeking a Clinical Research Coordinator to execute, manage, and coordinate pediatric research protocols under supervision. The role involves coordinating data collection, regulatory compliance, and study logistics across several concurrent studies.

The CRC will oversee data integrity, IRB submissions, staff training, and collaboration with physicians and study teams to ensure timely and accurate study progress while adhering to regulatory standards.