Top 3 Clinical research coordinator i (crc 1) Jobs in Chicago, Il

Clinical Research Coordinator I (CRC-1)
Insight —Chicago, IL
- $50,000 - $65,000 a year
- Full-time
- Nursing
- Hospital
- Organizational skills
Quick Apply
Clinical Research Coordinator Level 1
ICON Plc —Downers Grove, IL
- $42,600 - $53,250 a year
- Full-time
- Mid-level
- Office
- Bachelor's degree
- Disability insurance
- Health insurance
8d
Clinical Resource Coordinator 1
Hospital: Rush University Medical Center —Chicago, IL
- $23.12 - $36.41 an hour
- 8 hour shift
- Mid-level
- High school diploma or GED
- Pediatrics
5d

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Clinical Research Coordinator I (CRC-1)
Insight —Chicago, IL
Clinical research certification (CCRC, CCRP) eligible; certification expected within 18 months of hire. Bachelor's degree in life sciences, nursing, healthcare,…
$50,000 - $65,000 a year
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Clinical Research Coordinator I
Loyola University Chicago —Maywood, IL
Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms. Open Date 02/17/2026.
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Clinical Research Coordinator I (CRC-1)

Insight -
Chicago, IL

Quick Apply

Job Details

Full-time
$50,000 - $65,000 a year

Qualifications

Quality control corrective actions
Data integrity assurance
Community engagement experience
Nursing
Informed consent
Electronic health records (EHR) management
Operations coordination
Client rapport building
Patient management software
Filing
Corrective and preventive actions (CAPA)
Patient safety
Research project coordination
Data integrity and documentation
ICH guidelines
Collecting samples for laboratory testing
Clinical data entry
Informed consent procedures implementation
Organizational skills
Clinical trial patient safety management
Implementing research protocols
Patient recruitment
Bachelor's degree in nursing
Communication with regulatory authorities for clinical trials
Clinical research inspection readiness
Patient interaction
Patient education
Associate's degree
Ethical review application preparation
Communication skills

Full Job Description

Health Systems Clinical Research

JOB DESCRIPTION

Job Title:

Clinical Research Coordinator I

Department:

Clinical Research Operations

Location:

On-site (Insight Hospital & Medical Center – Chicago)

Schedule:

Full-time, Monday through Friday (8AM–5PM)

Reports To:

Director of Clinical Trials and Clinical Research Coordinator III – Team Lead

Position Summary

The Clinical Research Coordinator I (CRC I) is responsible for supporting the conduct of clinical trials under direct supervision from senior coordinators and the CRC III – Team Lead or the Director of Clinical Trials. The CRC I supports the coordination of study activities across all phases, including participant recruitment, screening, enrollment, and data collection. This role builds foundational skills in GCP, regulatory processes, and clinical trial operations while contributing to the overall success of the site's research portfolio. The CRC I collaborates with the Patient Recruitment department, regulatory resources, and the broader clinical research team to ensure protocol adherence, participant safety, and data integrity.

Core Competencies

Foundational knowledge of clinical trial operations, Good Clinical Practice (GCP), FDA regulations, and IRB processes
Strong organizational skills with attention to detail and the ability to manage multiple priorities under supervision
Effective communication and interpersonal skills with study participants, team members, and external stakeholders
Commitment to participant safety, data integrity, and regulatory compliance
Eagerness to learn, adapt, and grow within a fast-paced clinical research environment
Proficiency in electronic health record (EHR) systems; exposure to electronic data capture (EDC) and clinical trial management systems (CTMS) preferred

Key Responsibilities

Study Coordination

Coordinate assigned clinical trial activities under the direction of the CRC III – Team Lead/Site Director/Site Manager and Principal Investigator
Coordinate site preparation, study startup, participant screening, enrollment, and follow-up visits
Ensure protocol adherence, timely data entry, and accurate source documentation for assigned studies
Prepare for and support monitoring visits, audits, and sponsor interactions

Participant Interaction and Recruitment

Serve as a point of contact for study participants, providing education about the study and addressing questions
Obtain and document informed consent in compliance with ICH-GCP and IRB requirements
Conduct prescreening activities and coordinate with the Patient Recruitment department to support enrollment goals
Participate in community engagement and outreach activities as directed

Data Collection and Management

Collect, record, and maintain accurate clinical trial data, ensuring integrity and confidentiality of participant information
Enter data into EDC systems accurately and within sponsor-required timelines
Manage query resolution and data clarification as directed by the CRC III – Team Lead or sponsor monitors

Regulatory and Quality Support

Support preparation and submission of IRB documents, amendments, and safety reports
Support the maintenance of essential regulatory files and study documentation
Participate in internal quality assurance activities and assist with CAPA implementation as directed
Maintain compliance with GCP, institutional policies, and applicable regulatory requirements

Minimum Education and Experience

Bachelor's degree in life sciences, nursing, healthcare, or a related field preferred; associate's degree with relevant clinical experience considered
Zero to one year of experience in a clinical, research, or healthcare setting
Clinical research certification (CCRC, CCRP) eligible; certification expected within 18 months of hire

Qualifications

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
Proficiency in electronic health record (EHR) systems; familiarity with EDC and CTMS platforms preferred
Phlebotomy skills preferred
Ability to work both independently and collaboratively in a fast-paced environment
Professional references may be required

Quick Apply

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clinical research coordinator i (crc 1) jobs in chicago, il

Clinical Research Coordinator I (CRC-1)

Clinical Research Coordinator Level 1

Clinical Resource Coordinator 1

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