Clinical Research Coordinator II — Multi-Trial Coordination & Patient Care

University of Chicago; Town of Hyde Park (NY); Hybrid; USD 60,000 - 75,000; Full time

Benefits offered by this job

Benefits eligible

Job summary

The University of Chicago Comprehensive Cancer Center is seeking a Clinical Research Coordinator 2 (CRC2) to partner with the Principal Investigator (PI) and support daily trial activities. The CRC2 coordinates enrollment, data collection, informed consent, and regulatory documentation with limited supervision.

Responsibilities include subject screening, scheduling, educating patients about procedures, coordinating site visits, and ensuring protocol adherence while maintaining data integrity and

Qualifications

• Minimum 2–5 years of clinical research experience.
• College or university degree in a related field is required.
• Ability to work with PI and study team with limited supervision.

Responsibilities

• Manage all aspects of conducting clinical trials including screening, enrollment, and AE reports.
• Recruit and interview potential study patients under PI guidance.
• Coordinate startup through closeout, including informed consent and data collection.
• Educate patients about procedures and visit schedules.
• Ensure compliance with SOPs and federal regulations.
• Maintain accurate trial documentation and IRB submissions.

Skills

Strong communication

Organizational skills

Time management

Data management

MS Office

Education

College/university degree in related field

Bachelor's degree (preferred)

Tools

Microsoft Office

IRB submission knowledge

Job description

The University of Chicago Comprehensive Cancer Center is seeking a Clinical Research Coordinator 2 (CRC2) to partner with the Principal Investigator (PI) and support daily trial activities. The CRC2 coordinates enrollment, data collection, informed consent, and regulatory documentation with limited supervision.

Responsibilities include subject screening, scheduling, educating patients about procedures, coordinating site visits, and ensuring protocol adherence while maintaining data integrity and