Clinical Research Coordinator II — Endocrinology Trials

Biological Sciences Division at the University of Chicago; Chicago (IL); On-site; USD 60,000 - 75,000; Full time

Job summary

The University of Chicago's Biological Sciences Division, Endocrinology Section, seeks a Clinical Research Coordinator II to work with the PI Dr. Silvana Pannain. The CRCII will coordinate participant enrollment, data collection, and study logistics within NIH/academic research settings.

Responsibilities include obtaining informed consent, ensuring GCP compliance, coordinating visits, and assisting with regulatory submissions. A strong communication and organizational skill set is essential.

Qualifications

• Bachelor’s degree or higher is preferred.
• 2–5 years of related work experience.
• Clinical research experience or relevant experience is preferred.

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.
• Coordinate study visits, assessments, and follow-ups.
• Maintain documentation in compliance with Good Clinical Practice (GCP).
• Prepare study-related reports and assist in regulatory submissions as needed.
• Present study findings and participate in research meetings and training.

Skills

Communication skills

Oral communication

Written communication

Interpersonal skills

Attention to detail

Multi-tasking

Teamwork

Independent work

Stress management

Training others

Presentations

Education

Bachelor’s degree

College or university degree in a related field

Job description

The University of Chicago's Biological Sciences Division, Endocrinology Section, seeks a Clinical Research Coordinator II to work with the PI Dr. Silvana Pannain. The CRCII will coordinate participant enrollment, data collection, and study logistics within NIH/academic research settings.

Responsibilities include obtaining informed consent, ensuring GCP compliance, coordinating visits, and assisting with regulatory submissions. A strong communication and organizational skill set is essential.