Clinical Coordinator Jobs in Chicago, IL
Clinical Coordinator jobs in Chicago are concentrated in the Medical District, Streeterville, and Hyde Park, with strong demand across hospital systems, outpatient clinics, and academic medical centers. Employers actively hiring include Rush University Medical Center, Northwestern Medicine, and INSIGHT. See the openings below and apply to the ones that match your experience.
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Showing 4 of 99+ Clinical Coordinator jobs
Location: Chicago, Illinois
Business Unit: Rush Medical Center
Hospital: Rush University Medical Center
Department: Neurological Sciences-Res Adm
Work Type: Full Time (Total FTE between 0.9 and 1.0)
Shift: Shift 1
Work Schedule: 8 Hr (7:00:00 AM - 3:00:00 PM)
Rush offers exceptional rewards and benefits learn more at our Rush benefits page (https://www.rush.edu/rush-careers/employee-benefits).
Pay Range: $27.47 - $38.81 per hour
Rush salaries are determined by many factors including, but not limited to, education, job-related experience and skills, as well as internal equity and industry specific market data. The pay range for each role reflects Rush’s anticipated wage or salary reasonably expected to be offered for the position. Offers may vary depending on the circumstances of each case.
Job Summary:
The Clinical Research Coordinator II (CRC II) independently coordinates assigned aspects of clinical research studies across a range of disciplines. Responsibilities include participant recruitment and retention, study data management, regulatory documentation submission and maintenance, communication with sponsors and institutional stakeholders, and monitoring of study compliance. The CRC II executes study protocols with increasing independence, identifies and resolves routine operational issues, contributes to process improvements, and may assist in mentoring less experienced staff.
Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.
Education:
- Bachelor’s degree
- 2+ years of experience coordinating clinical trials
- Independent site management experience
Experience (in lieu of a degree)
- 3 years total experience in coordinating clinical trials with increasing complexity
Knowledge, Skills, & Abilities:
- Regulatory Knowledge – Understands Good Clinical Practices (GCP) and proper research documentation.
- Regulatory Compliance – Knows the basic rules and guidelines from NIH and FDA that apply to research.
- Project & Time Management – Can manage timelines, keep track of tasks, and handle several study activities at once.
- Problem-Solving & Judgment – Can figure out solutions when challenges come up and make thoughtful decisions.
- Detail & Organization – Pays close attention to detail and keeps study data and records well organized.
- Participant & Vendor Interaction – Builds trust with participants and communicates respectfully with sponsors and outside partners.
- Communication Skills – Speaks and writes clearly when sharing information with research teams, participants, or external groups.
- Teamwork – Works well with other staff and helps solve problems as part of the team.
- Flexibility – Willing to work evenings or weekends if the study requires it.
- Travel Readiness – Able to travel locally or nearby for study visits, participant support, or training.
Preferred Job Qualifications:
Experience:
- 2-5 years’ experience in clinical research conduct, regulatory management, or research administration
Certifications:
- Relevant certification strongly preferred (Certified Clinical Research Professionals (CCRP),
- Certified Clinical Research Associate (CCRA),
- Certified Clinical Research Coordinator (CCRC), OR
- Certified IRB Professional (CIP)
Job Responsibilities:
1. Coordinates all aspects of the study including recruitment, consent, screening, scheduling, tracking, and provides study updates to study participants throughout the conduct of the study.
2. May collect and enter data into study case report forms and/or electronic data capture system and respond to queries in a timely manner.
3. Independently submits or partners with a regulatory coordinator to submit study related documents, study protocols, and study protocol amendments to the IRB per policy and procedure, with increasing autonomy over time to prepare for independent regulatory management responsibilities.
4. Ensures procedural documentation is accurate, complete, and in compliance with institutional, local, state, and federal guidelines and regulations related to clinical research.
5. Verifies and ensures that data is consistent with 100% of source documentation before entry into case report forms and electronic data capture systems to support accuracy, timeliness, and audit readiness.
6. May collect, process, and ship potentially biohazardous specimens.
7. May administer more complex structured tests and questionnaires according to research study protocols, including providing protocol-specific education to participants regarding procedures and expectations. May utilize study-related technology and equipment as part of assessment procedures.
8. Provides ongoing study status updates, responds to questions, and may create summary report(s) for distribution to the PI, Administrator, department stakeholders, Sponsor, and Compliance throughout the conduct of the study.
9. Organizes and participates in auditing and monitoring visits.
10. Monitors participant interactions for protocol deviations, adverse events (AEs), and serious adverse events (SAEs), and reports findings per institutional and regulatory guidelines.
11. Partners with PI(s), sponsor, compliance, clinical staff, and manager to identify and improve more complex processes as it relates to the conduct of the research study.
12. May provide oversight, training, and coaching to less experienced staff.
13. Other duties as assigned.
Rush is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
Location: Chicago, Illinois
Business Unit: Rush Medical Center
Hospital: Rush University Medical Center
Department: Neurological Sciences-Res Adm
Work Type: Full Time (Total FTE between 0.9 and 1.0)
Shift: Shift 1
Work Schedule: 8 Hr (7:00:00 AM - 3:00:00 PM)
Rush offers exceptional rewards and benefits learn more at our Rush benefits page (https://www.rush.edu/rush-careers/employee-benefits).
Pay Range: $27.47 - $38.81 per hour
Rush salaries are determined by many factors including, but not limited to, education, job-related experience and skills, as well as internal equity and industry specific market data. The pay range for each role reflects Rush’s anticipated wage or salary reasonably expected to be offered for the position. Offers may vary depending on the circumstances of each case.
Job Summary:
The Clinical Research Coordinator II (CRC II) independently coordinates assigned aspects of clinical research studies across a range of disciplines. Responsibilities include participant recruitment and retention, study data management, regulatory documentation submission and maintenance, communication with sponsors and institutional stakeholders, and monitoring of study compliance. The CRC II executes study protocols with increasing independence, identifies and resolves routine operational issues, contributes to process improvements, and may assist in mentoring less experienced staff.
Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.
Education:
- Bachelor’s degree
- 2+ years of experience coordinating clinical trials
- Independent site management experience
Experience (in lieu of a degree)
- 3 years total experience in coordinating clinical trials with increasing complexity
Knowledge, Skills, & Abilities:
- Regulatory Knowledge – Understands Good Clinical Practices (GCP) and proper research documentation.
- Regulatory Compliance – Knows the basic rules and guidelines from NIH and FDA that apply to research.
- Project & Time Management – Can manage timelines, keep track of tasks, and handle several study activities at once.
- Problem-Solving & Judgment – Can figure out solutions when challenges come up and make thoughtful decisions.
- Detail & Organization – Pays close attention to detail and keeps study data and records well organized.
- Participant & Vendor Interaction – Builds trust with participants and communicates respectfully with sponsors and outside partners.
- Communication Skills – Speaks and writes clearly when sharing information with research teams, participants, or external groups.
- Teamwork – Works well with other staff and helps solve problems as part of the team.
- Flexibility – Willing to work evenings or weekends if the study requires it.
- Travel Readiness – Able to travel locally or nearby for study visits, participant support, or training.
Preferred Job Qualifications:
Experience:
- 2-5 years’ experience in clinical research conduct, regulatory management, or research administration
Certifications:
- Relevant certification strongly preferred (Certified Clinical Research Professionals (CCRP),
- Certified Clinical Research Associate (CCRA),
- Certified Clinical Research Coordinator (CCRC), OR
- Certified IRB Professional (CIP)
Job Responsibilities:
1. Coordinates all aspects of the study including recruitment, consent, screening, scheduling, tracking, and provides study updates to study participants throughout the conduct of the study.
2. May collect and enter data into study case report forms and/or electronic data capture system and respond to queries in a timely manner.
3. Independently submits or partners with a regulatory coordinator to submit study related documents, study protocols, and study protocol amendments to the IRB per policy and procedure, with increasing autonomy over time to prepare for independent regulatory management responsibilities.
4. Ensures procedural documentation is accurate, complete, and in compliance with institutional, local, state, and federal guidelines and regulations related to clinical research.
5. Verifies and ensures that data is consistent with 100% of source documentation before entry into case report forms and electronic data capture systems to support accuracy, timeliness, and audit readiness.
6. May collect, process, and ship potentially biohazardous specimens.
7. May administer more complex structured tests and questionnaires according to research study protocols, including providing protocol-specific education to participants regarding procedures and expectations. May utilize study-related technology and equipment as part of assessment procedures.
8. Provides ongoing study status updates, responds to questions, and may create summary report(s) for distribution to the PI, Administrator, department stakeholders, Sponsor, and Compliance throughout the conduct of the study.
9. Organizes and participates in auditing and monitoring visits.
10. Monitors participant interactions for protocol deviations, adverse events (AEs), and serious adverse events (SAEs), and reports findings per institutional and regulatory guidelines.
11. Partners with PI(s), sponsor, compliance, clinical staff, and manager to identify and improve more complex processes as it relates to the conduct of the research study.
12. May provide oversight, training, and coaching to less experienced staff.
13. Other duties as assigned.
Rush is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
See All 99 Clinical Coordinator Jobs in Chicago
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Find Clinical Coordinator JobsClinical Coordinator Job Market in Chicago
Who's Hiring
- Rush University Medical Center26
- Northwestern Medicine14
- INSIGHT8
- Sinai Chicago8
- The IMA4
Top Industries Hiring
- Healthcare & Medical Services16
- Education10
- Distribution & Wholesale2
- Transportation & Logistics2
Clinical Coordinator Jobs in Chicago: Frequently Asked Questions
How do I get a clinical coordinator job in Chicago?
Focus your search on Chicago's major medical corridors: the Illinois Medical District on the Near West Side, Streeterville's hospital cluster along the lakefront, and the University of Chicago Medicine complex in Hyde Park. Large academic health systems, federally qualified health centers, and specialty outpatient groups hire the most. Candidates with experience in care coordination, prior authorization, or clinical trial support stand out in this market.
Which companies hire clinical coordinators in Chicago?
Companies currently hiring clinical coordinators in Chicago include Rush University Medical Center, Northwestern Medicine, and INSIGHT, per current listings on Migrate Mate as of August 2026. Chicago's hiring landscape is anchored by large academic medical centers, multi-site outpatient networks, and research institutions that maintain steady coordinator demand throughout the year.
Are there remote clinical coordinator jobs in Chicago?
Yes, though remote availability is limited for hands-on, patient-facing roles and more common for desk-based functions like care management, utilization review, and clinical trial coordination. About 25% of clinical coordinator openings tied to Chicago are remote or hybrid as of August 2026, reflecting a mix of telehealth and administrative positions. Care management and documentation-heavy coordinator roles see the most remote flexibility locally.
How can I get a clinical coordinator job in Chicago with little or no experience?
The most realistic entry path in Chicago is through a medical assistant, patient care technician, or health unit coordinator role at one of the city's large hospital systems, which routinely promote internally into coordinator positions. Federally qualified health centers and community health organizations in neighborhoods like Pilsen and Roseland also hire entry-level coordinators. Familiarity with Epic or Cerner and a CNA or phlebotomy certification sharpens a candidate's profile significantly in Chicago's competitive market.
Which industries hire the most clinical coordinators in Chicago?
Chicago clinical coordinator roles concentrate in Healthcare & Medical Services, Education, and Distribution & Wholesale, based on current listings on Migrate Mate as of August 2026. Chicago's density of academic medical centers, specialty research hospitals, and a growing outpatient and telehealth sector makes it one of the stronger markets for coordinator hiring in the Midwest.
See All 99 Clinical Coordinator Jobs in Chicago
Find roles in Chicago that match your experience and apply in just a few clicks.
Find Clinical Coordinator Jobs