Clinical Research Coordinator Ii - Obg - Research Staff
University of Chicago
Chicago, IL, US
Base: $60,000.00 - $75,000.00; bonus/equity: not s...
2-5 years work experience
Irb protocol development and amendments
Patient recruitment and consent procedures
The role independently manages and executes moderately complex clinical research studies from start up through close out while ensuring scientific integrity and regulatory compliance
Job Summary
The role independently manages and executes moderately complex clinical research studies from start up through close out while ensuring scientific integrity and regulatory compliance.
Candidates will perform technical laboratory duties including cell culturing, DNA extraction, PCR, and ELISA alongside clinical data management and patient recruitment.
The University of Chicago offers a comprehensive benefits package including health, retirement, and paid time off for eligible employees.
Matching Summary
The role independently manages and executes moderately complex clinical research studies from start up through close out while ensuring scientific integrity and regulatory compliance.
Salary
Base: $60,000.00 - $75,000.00; Bonus/Equity: Not specified; Benefits: Health, retirement, and paid time off included
Skills & Requirements
Must-have
2-5 years work experience
IRB protocol development and amendments
Patient recruitment and consent procedures
Biological sample collection and processing
Data management using REDCap or Excel
Nice-to-have
Experience with NIH sponsor reporting
Manuscript writing and publication skills
Animal care and study design knowledge
Multidisciplinary team collaboration
Troubleshooting specialized laboratory machinery
Key Requirements
College degree in related field
2-5 years of related work experience
Knowledge of IRB processes and federal regulations
Ability to exercise professional judgment on study logistics