Clinical Research Coordinator I (CRC-1)
On-siteChicago, Illinois, United States
Job Summary
Coordinate assigned clinical trial activities including site preparation, participant screening, enrollment, and follow-up visits under the direction of senior coordinators. Serve as a point of contact for study participants to provide education, obtain informed consent, and conduct prescreening activities. Collect and enter accurate clinical trial data into electronic data capture systems while managing query resolution and ensuring source documentation integrity. Support preparation of regulatory documents, safety reports, and monitoring visits to maintain compliance with GCP and IRB requirements. Full-time, Monday through Friday (8AM–5PM) at Insight Hospital & Medical Center in Chicago.
Required Qualifications
- Bachelor's degree in life sciences, nursing, healthcare, or a related field
- Associate's degree with relevant clinical experience
- Zero to one year of experience in a clinical, research, or healthcare setting
- Clinical research certification (CCRC, CCRP) eligible
- Strong understanding of or willingness to learn clinical trial processes and the regulatory environment
- Minimum 1 year experience supporting clinical research study coordination at the site level
- Excellent organizational skills and attention to detail, with the ability to manage multiple priorities and deadlines
- Strong interpersonal and communication skills, with the ability to build rapport with participants and collaborate effectively with team members
- Ability to work both independently and collaboratively in a fast-paced environment
Desired Qualifications
- Proficiency in electronic health record (EHR) systems
- Exposure to electronic data capture (EDC) and clinical trial management systems (CTMS)
- Clinical research certification (CCRC, CCRP)
- Certification expected within 18 months of hire
- Phlebotomy skills
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