| Location | Chicago, IL |
| Salary | $61,730–$71,647 Per Year |
Job Description - CLINICAL RESEARCH COORDINATOR (00139542)
Job Description
CLINICAL RESEARCH COORDINATOR
Requisition ID
: 00139542
Job Posting
: Sep 16, 2026, 9:21:16 PM
Closing Date
: Oct 1, 2026, 10:29:00 AM Full-time Shift Start Time: 8:00 A.M. Shift End Time: 4:00 P.M.
Posting Salary: $61,730 - $71,647
Organization
: Health and Hospital Systems
This position is exempt from Career Service under the CCH Personnel Rules.
Salary is commensurate with years of experience indicated at time of application submittal. Experience not disclosed or documented at the time of application will not be considered for initial step placement.
Job Summary
The Clinical Research Coordinator assists with the study recruitment process, including screening and obtaining consents from eligible candidates. Supports study conduct throughout the lifecycle of the study. Supports and maintains the integrity and quality of clinical research, by ensuring that research is conducted in accordance with Good Clinical Practice (GCP) Guidelines, federal and sponsor regulations and guidelines, institutional policies and procedures, and study protocol.
Typical Duties
Maintains accurate and timely documentation and actively communications with investigators, colleagues, study participants, sponsors, IRB, and other research related entities as needed.
Ensures study-related procedures are executed per protocol and performed in accordance with protocol timelines.
Participates in study recruitment, including identifying and screening research participants for study eligibility
Implements processes to ensure study-related procedures are executed per protocol and performed in accordance with protocol timelines
Obtains consent from research participants and ensures participants understand the protocol and what is expected of them while participating
Identifies adverse events based on gained knowledge and reports them in a timely and accurate manner to the principal investigator and appropriate regulatory authorities (IRB, sponsor, etc.)
Maintains source documents in accordance with institutional procedures
Packages and ships study-related specimen and/or samples in accordance with Cook County Health System, International Air Transport Association (IATA) and sponsor guidelines
Obtains and organizes supplies needed to complete study tasks
Proactively identifies and participates in training, continuing education, and development activities to broaden knowledge and enhance professional development
Keeps up to date on relevant State and Federal research guidelines and regulations
Manages risk to the organization(s) and principal investigators by ensuring up-to-date training and compliance in accordance with complex state and federal regulatory statues and rules
Manages variety of work requiring critical attention to detail and prioritization
Minimum Qualifications
Associate degree from an accredited college or university or higher
Two (2) years in a clinical research or relevant experience
Proficiency using Microsoft Office (Excel and Word)
Preferred Qualifications
Bachelor's degree from an accredited college or university
Knowledge, Skills, Abilities and Other Characteristics
Knowledge of medical terminology
Knowledge of GCP concepts
Knowledge in setting up, coordinating, and managing clinical research studies
Knowledge and understanding of policies, procedures, and regulations governing human subject research
Knowledge and understanding of the Federal regulations and guidelines governing the protection of human subjects (e.g., FDA, OHRP, GCP/ICH guidelines, and HIPAA regulations) prior to interacting with research subjects
Knowledge of components of clinical research operations, including study implementation, oversight, and coordination
Knowledge of CRF completion, and documentation standards, including timely and accurate transcription of study data
Ability to analyze, organize, and prioritize work under pressure while meeting deadlines
Ability to maintain confidentiality
Skill in completing assignments accurately and with attention to detail
Excellent interpersonal, written, and verbal communication skills
Ability to work independently and/or in a collaborative environment
Proficient in understanding phases of clinical trials
Demonstrate an understanding of clinical research compliance
VETERAN PREFERENCE
PLEASE READ
When applying for employment with the Cook County Health & Hospitals System, preference is given to honorably discharged Veterans who have served in the Armed Forces of the United States for not less than 6 months of continuous service
To take advantage of this preference a Veteran must:
Discharge papers must list an Honorable Discharge Status. Discharge papers not listing an Honorable Discharge Status are not acceptable
OR
A copy of a valid State ID Card or Driver's License which identifies the holder of the ID as a Veteran, may also be attached to the application at time of filing.
If items are not attached, you will not be eligible for Veteran Preference
VETERANS MUST PROVIDE ORIGINAL APPLICABLE DISCHARGE PAPERS OR APPLICABLE STATE ID CARD OR DRIVER'S LICENSE AT TIME OF INTERVIEW.
Benefits Package
For further information on our excellent benefits package, please click on the following link: http://www.cookcountyrisk.com/
COOK COUNTY HEALTH & HOSPITALS SYSTEM IS AN EQUAL OPPORTUNITY EMPLOYER