Clinical Research Coordinator II - Endocrinology Trials

uchicago; Austin (TX); On-site; USD 60,000 - 75,000; Full time

Job summary

The University of Chicago seeks a Clinical Research Coordinator II (CRCII) to partner with the clinical PI, Dr. Silvana Pannain, in the Endocrinology section.

The role entails coordinating trials in a leading NIH-funded environment, enrolling participants, and ensuring compliant data collection and reporting. Responsibilities include consent, participant education, regulatory submissions, and cross-functional collaboration with researchers and staff.

Qualifications

• 2–5 years of work experience in a related job discipline.
• Familiarity with Good Clinical Practice (GCP) and regulatory requirements.

Responsibilities

• Recruit, screen, and enroll eligible study participants.
• Obtain informed consent and provide detailed study information to patients.
• Monitor patient status, collect clinical data, and report adverse events.
• Collect biospecimens according to protocol.
• Maintain accurate and timely documentation in compliance with GCP.
• Coordinate study visits, assessments, and follow-ups.
• Educate patients and families about clinical trials and research procedures.
• Ensure adherence to ethical guidelines, regulatory requirements, and institutional policies.
• Collaborate with investigators, study coordinators, and other healthcare staff.
• Prepare study-related reports and assist in regulatory submissions when needed.
• Present study findings and participate in research meetings and training as needed.
• Facilitate daily activities of moderately complex clinical studies and perform related tasks.
• Accountable for all tasks in moderately complex clinical studies.
• Performs other related work as needed.

Skills

Clinical research coordination

Education

College/University degree in related field

Bachelor's degree

Job description

The University of Chicago seeks a Clinical Research Coordinator II (CRCII) to partner with the clinical PI, Dr. Silvana Pannain, in the Endocrinology section.

The role entails coordinating trials in a leading NIH-funded environment, enrolling participants, and ensuring compliant data collection and reporting. Responsibilities include consent, participant education, regulatory submissions, and cross-functional collaboration with researchers and staff.