Base: $60,000.00 - $75,000.00; bonus/equity: not s...
2-5 years clinical research experience
Informed consent process management
Irb submission and review facilitation
The Clinical Research Coordinator 2 supports the Principal Investigator in managing all aspects of moderately complex clinical trials from startup through closeout
Job Summary
The Clinical Research Coordinator 2 supports the Principal Investigator in managing all aspects of moderately complex clinical trials from startup through closeout.
This role requires independent execution of daily activities including patient recruitment, informed consent collection, specimen processing, and adverse event monitoring.
The University of Chicago offers a competitive salary range of $60,000.00 - $75,000.00 along with comprehensive health, retirement, and paid time off benefits.
Matching Summary
The Clinical Research Coordinator 2 supports the Principal Investigator in managing all aspects of moderately complex clinical trials from startup through closeout.
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 clinical research experience
informed consent process management
IRB submission and review facilitation
adverse event reporting and monitoring
case report form completion
protocol adherence and compliance
Nice-to-have
experience with multi-site trials
ability to train new coordinators
strong interpersonal relationship skills
confidentiality and discretion handling
presentation delivery capabilities
Key Requirements
College or university degree in related field
2-5 years work experience in related discipline
Bachelor's degree preferred
Knowledge of federal regulations and IRB processes