University of Chicago·Chicago, Illinois
The CRC2 coordinates daily clinical trial activities, including patient screening, enrollment, and specimen collection under the direction of a Principal Investigator. They manage regulatory compliance, IRB submissions, and maintain accurate study records from startup through closeout.
BSD MED - Hematology and Oncology - Clinical Research Staff - Cluster 9
About the Department
The Section of Hematology/Oncology has a proud and long tradition of excellence in research-based patient care and clinical discovery. Ranked among the finest cancer programs in the country, the Section is comprised of nationally and internationally known faculty with expertise in all major types of malignancies, blood disorders, and experimental therapies.
The Clinical Research Coordinator II (CRC2) is a specialized researcher partnering with the clinical Principal Investigator (PI) and under the direction of a departmental or lab research manager. While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC2 supports, facilitates and coordinates independently the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties with limited supervision and/or guidance, the CRC2 works with the PI, department, sponsor, and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.
Minimum requirements include a college or university degree in related field.
Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline.
Certifications: ---
• Bachelors degree.
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When applying, the document(s) MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.
37.5
$60,000.00 - $75,000.00
The included pay rate or range represents the University’s good faith estimate of the possible compensation offer for this role at the time of posting.
Benefits: Eligible
The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in the http://mybenefits.nfp.com/UChicago/benefits-guide/Benefits Guidebook [http://mybenefits.nfp.com/UChicago/benefits-guide/]. [http://mybenefits.nfp.com/UChicago/benefits-guide/]
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Requires a college or university degree in a related field and 2-5 years of experience in a related job discipline. A bachelor's degree and experience coordinating multiple industry-sponsored or multi-site trials are preferred.
Market context
Clinical Research Coordinator II roles in hematology/oncology are often in demand in Illinois because cancer studies rely on experienced coordinators who can manage protocol compliance, patient visits, and sponsor communication. This category is competitive when employers prefer a bachelor’s degree and prior coordination of industry-sponsored or multi-site trials. Review the AI-summarized requirements and benefits on this platform to save time, then match your experience with trial coordination, regulatory documentation, and patient-facing research workflows before applying.