Endocrinology Clinical Research Coordinator II

The University Of Chicago; Chicago (IL); On-site; USD 60,000 - 75,000; Full time

Job summary

The Clinical Research Coordinator II (CRCII) at The University Of Chicago partners with the Principal Investigator in the Endocrinology section to recruit, consent, and monitor study participants, collect data and specimens, and ensure adherence to GCP and all regulatory guidelines.

They coordinate visits, educate patients, and assist with regulatory submissions while maintaining accurate documentation and reporting in a busy clinical research setting.

Qualifications

• College or university degree is required.
• 2–5 years of related work experience in clinical research or related field.
• Experience coordinating studies (investigator-initiated, industry-sponsored, multi-site) preferred.

Responsibilities

• Recruit, screen, and enroll eligible participants.
• Obtain informed consent and provide study information to participants.
• Monitor participant status and collect clinical data.
• Collect biospecimens per protocol and ensure proper documentation (GCP compliant).
• Coordinate study visits and follow-ups, educate participants and families about trials.
• Ensure regulatory adherence and assist with submissions as needed.
• Present findings and participate in research meetings and training.

Skills

Clinical research

Regulatory compliance

Data collection

Informed consent

GCP awareness

Education

Bachelor's degree

Job description

The Clinical Research Coordinator II (CRCII) at The University Of Chicago partners with the Principal Investigator in the Endocrinology section to recruit, consent, and monitor study participants, collect data and specimens, and ensure adherence to GCP and all regulatory guidelines.

They coordinate visits, educate patients, and assist with regulatory submissions while maintaining accurate documentation and reporting in a busy clinical research setting.