Clinical Research Coordinator II

Carle Health

. Promote good clinical practices in the conduct of clinical investigations .

Posted 10/1/2026full-timePeoria • Illinois • United StatesMid-LevelSenior💰 $25 - $42 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in coordinating clinical research studies while ensuring compliance with regulatory requirements and Good Clinical Practices (GCP). Proficient in data management, informed consent processes, and effective communication with research teams and subjects.

Highest-signal resume keywords

Certified Clinical Research Coordinator (CCRC)Good Clinical Practices (GCP)Federal Regulations KnowledgeClinical Trial Data ManagementInformed Consent Procedures

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial CoordinationProtocol ComplianceData CollectionSource Document MaintenanceCase Report Form PreparationSubject Eligibility AssessmentEnrollment MonitoringSpecimen CollectionAdverse Event ReportingRegulatory Document Submission

Soft Skills

Effective CommunicationPatient EducationTeam CollaborationProblem SolvingAttention to Detail

Tools & Technologies

Electronic Data Capture (EDC)Interactive Voice Response System (IVRS)Clinical Trial Management Systems (CTMS)

Certifications & Qualifications

Certified Clinical Research Coordinator (CCRC)

Industry Keywords

Institutional Review Boards (IRBs)FDA Code of Federal Regulations (CFR)International Conference on Harmonization (ICH)Human Subject ProtectionClinical Investigations

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Promote good clinical practices in the conduct of clinical investigations
Assure compliance with protocol and regulatory requirements
Review technical operations and ensure processes, protocols, and procedures are quality controlled
Coordinate assigned research studies at all levels of acuity within the scope of licensure
Plan and design forms and source-document tools for protocol implementation
Document protocol deviations and exemptions
Obtain, review, abstract, record, correct, and maintain source documents and case report form data
Key and transmit electronic study data and resolve data queries
Maintain study article dispensing logs and study-related files
Prepare case report forms and source documents for sponsor or audit review
Monitor enrollment goals and modify recruitment plans as needed
Maintain screening and enrollment logs and follow patient populations clinically
Review eligibility criteria and required medical-record documentation with investigators
Explain protocols, informed consent forms, and follow-up procedures to potential subjects
Conduct subject interviews and obtain informed consent before study procedures
Follow randomization procedures and assure study-article administration
Schedule follow-up visits and review subject diaries and questionnaires
Ensure specimen collection, batching, and shipping
Assess subject compliance and report laboratory values or alerts to investigators and sponsors
Protect patient privacy and securely store or dispose of sensitive documents
Communicate with subjects, research teams, IRBs, sponsors, CROs, primary care providers, and monitors
Submit protocol amendments, progress reports, regulatory documents, and adverse-event notifications within required timeframes
Schedule and participate in sponsor monitoring visits
Clarify enrollment, sponsor-expectation, and study-procedure questions with investigators and sponsors
Integrate proposed clinical trials with current research activities
Attend investigator meetings and confirm required approvals and informed-consent documents before study initiation
Educate patients on medication or device use in the study
Provide management feedback on integrating research operations into clinic workflows

Requirements

What you’ll need

Coordinates assigned research studies within the scope of licensure
In-depth knowledge of federal regulations and guidance documents for clinical trials and human subject protection
Knowledge of Good Clinical Practices (GCP), local, state, and federal laws, regulations, guidance, policies, and procedures
Knowledge of Institutional Review Boards (IRBs), FDA Code of Federal Regulations (CFR), and International Conference on Harmonization (ICH) requirements
High school diploma/GED required
Bachelor's degree in a related field listed as an education qualification
Certified Clinical Research Coordinator (CCRC) within 2.5 years through the Association of Clinical Research Professionals (ACRP)
Completion of sponsored protocol training, including GCP, EDC, IVRS, and IRB
Ability to conduct informed consent, assess subject eligibility, and follow protocol procedures
Ability to collect, record, maintain, and transmit accurate clinical trial data and source documentation

Benefits

Comp & perks

Comprehensive benefits package
Equal Opportunity Employer
Potential for growth and life-long careers