Pediatric Clinical Research Coord II – On-Site (Part-Time)

Shriners Children’s Hospital; Sacramento (CA); Hybrid; USD 45,000 - 67,000; Part time

Job summary

Shriner's Children’s Hospital seeks a Clinical Research Coordinator II (CRC2) for a part-time, on-site role in Sacramento, CA. The CRC2 coordinates regulatory compliance, study operations, and data management under the Clinical Research Program Manager and SHC leadership, supporting pediatric clinical research activities.

Preferred candidates have 5+ years in clinical research administration, 3+ years in site management and IRB/regulatory work, and familiarity with GCP, ethics, and data

Qualifications

• 5+ years of specific experience in the administration of clinical research
• 3+ years in site/study management, IRBs, and regulatory compliance
• Experience with electronic health systems and databases used in research environments
• Knowledge of regulations related to clinical research, consent, protocol, and sponsor policies

Responsibilities

• Maintain knowledge of clinical research regulatory requirements
• Track study, investigator, IRB information, patient recruitment, and finances
• Coordinate collection, analysis, and dissemination of data results
• Prepare and analyze study results for the research team
• Maintain Belmont Report, Nuremberg Code, and ICH GCP standards
• Protect patient safety and privacy throughout the study
• Collaborate with SHC leadership to uphold research mission
• Ensure scientific integrity and ethical conduct

Skills

Clinical research administration

IRB regulations

GCP guidelines

Patient recruitment

Data management

Education

Bachelor's degree in clinical research or related field

CCRP or CCRC certification

Tools

Electronic health record systems

Job description

Shriner's Children’s Hospital seeks a Clinical Research Coordinator II (CRC2) for a part-time, on-site role in Sacramento, CA. The CRC2 coordinates regulatory compliance, study operations, and data management under the Clinical Research Program Manager and SHC leadership, supporting pediatric clinical research activities.

Preferred candidates have 5+ years in clinical research administration, 3+ years in site management and IRB/regulatory work, and familiarity with GCP, ethics, and data