Barrington James
Clinical Research Coordinator (CRC) — 6-Month Contract (Contract-to-Hire Opportunity)
Southwest Chicago Area
We are seeking an experienced Clinical Research Coordinator for immediate contract placement at one of our clinical research sites in the region. This role is a 6‑month contract with the option to become a permanent position. Applicants must be eligible to work in the United States and require no current or future sponsorship.
Requirements
Valid GCP and IATA certifications
Minimum 1 year of hands‑on experience in clinical research coordination
Core Responsibilities
Maintain regulatory files (Investigator Site File)
Work with IRBs on submissions, reviews, and regulatory correspondence
Recruit and screen participants for clinical trials
Manage the informed consent process according to ICH and GCP standards
Perform and document study assessments per protocol using ALCOA‑CCC principles
Conduct phlebotomy; process and ship blood and urine samples following study protocols
Enter source data and respond to queries in EDC systems (such as Medidata RAVE)
Perform study assessments including vitals, ECGs, and other protocol procedures
Document and follow up on adverse events and serious adverse events in line with sponsor requirements
Dispense and collect investigational products; maintain accountability and temperature logs; report temperature excursions; work with IRT systems
Schedule and participate in sponsor/CRO visits including QV, SIV, IMV, and COV
If you meet these qualifications and are available for immediate placement, please reach out to learn more about this opportunity.
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We are seeking an experienced Clinical Research Coordinator for immediate contract placement at one of our clinical research sites in the region. This role is a 6‑month contract with the option to become a permanent position. Applicants must be eligible to work in the United States and require no current or future sponsorship.
Requirements
Valid GCP and IATA certifications
Minimum 1 year of hands‑on experience in clinical research coordination
Core Responsibilities
Maintain regulatory files (Investigator Site File)
Work with IRBs on submissions, reviews, and regulatory correspondence
Recruit and screen participants for clinical trials
Manage the informed consent process according to ICH and GCP standards
Perform and document study assessments per protocol using ALCOA‑CCC principles
Conduct phlebotomy; process and ship blood and urine samples following study protocols
Enter source data and respond to queries in EDC systems (such as Medidata RAVE)
Perform study assessments including vitals, ECGs, and other protocol procedures
Document and follow up on adverse events and serious adverse events in line with sponsor requirements
Dispense and collect investigational products; maintain accountability and temperature logs; report temperature excursions; work with IRT systems
Schedule and participate in sponsor/CRO visits including QV, SIV, IMV, and COV
If you meet these qualifications and are available for immediate placement, please reach out to learn more about this opportunity.
#J-18808-Ljbffr