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Full Time Redcap Jobs in Chicago, IL (NOW HIRING)

Research Coordinator-ILPQC

Evanston, IL · On-site

$24.86 - $37.29/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Evanston, IL * Full Time/Part Time: Full Time, hybrid schedule * Hours: 8am-4:30pm * Required ... Experience working with data management systems and software such as REDCap, SPSS, Ripple.

Research Coordinator-ILPQC

Evanston, IL

$24.86 - $37.29/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Evanston, IL * Full Time/Part Time: Full Time, hybrid schedule * Hours: 8am-4:30pm * Required ... Experience working with data management systems and software such as REDCap, SPSS, Ripple.

Workforce Associate

Chicago, IL

$46K - $50K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

We are now hiring for a full-time Workforce Associate to join our Calumet Team! SALARY: * The ... into RedCap, Salesforce, Illinois Worknet, and other funder provided databases. * Receives ...

Workforce Associate

Chicago, IL · On-site

$46K - $50K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

We are now hiring for a full-time Workforce Associate to join our Calumet Team! SALARY: * The ... into RedCap, Salesforce, Illinois Worknet, and other funder provided databases. * Receives ...

Full Time Redcap information

See Chicago, IL salary details

$18

$30

$50

How much do full time redcap jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for full time redcap in Chicago, IL is $30.90, according to ZipRecruiter salary data. Most workers in this role earn between $23.75 and $34.66 per hour, depending on experience, location, and employer.

What is the difference between Full Time Redcap vs Clinical Data Coordinator?

AspectFull Time RedcapClinical Data Coordinator
Required CredentialsExperience with Redcap, data management skillsOften similar, may include certifications in clinical research
Work EnvironmentResearch settings, clinical trials, academic institutionsHospitals, research organizations, clinical sites
Employer & IndustryResearch institutions, universities, pharma companiesHealthcare providers, research hospitals
Common Search & ComparisonRedcap expertise, data management rolesClinical data management, research coordination

Full Time Redcap and Clinical Data Coordinator roles often overlap in data management and research environments. While both require knowledge of clinical data systems, Full Time Redcap focuses specifically on managing and maintaining Redcap databases, whereas Clinical Data Coordinators handle broader data collection, quality control, and coordination tasks across clinical studies.

What are the most commonly searched types of Redcap jobs in Chicago, IL?

The most popular types of Redcap jobs in Chicago, IL are:

Infographic showing various Full Time Redcap job openings in Chicago, IL as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 81% Full Time, 13% Part Time, 1% Temporary, and 3% Contract. Highlights an 89% Physical, 6% Hybrid, and 5% Remote job distribution, with an average salary of $64,271 per year, or $30.9 per hour.

Clinical Research Coordinator

ECN Operating LLC

Merrillville, IN • On-site

$23.75 - $31.75/hr

Full-time

Posted 14 days ago


Job description

Job Summary:

We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include specimen collection and basic clinical procedures.

Key Responsibilities:

  • Coordinate day-to-day clinical research activities to ensure study protocols are followed.
  • Recruit, screen, and enroll study participants.
  • Obtain informed consent and ensure ethical conduct in all study interactions.
  • Collect, process, and ship biological specimens per protocol (e.g., blood draws, urine samples).
  • Perform basic clinical procedures as permitted by certification (e.g., vital signs, EKGs).
  • Maintain accurate and timely documentation in case report forms and electronic databases.
  • Communicate with sponsors, monitors, and IRBs regarding study progress and compliance.
  • Schedule participant visits and follow-ups; ensure visit windows are met.
  • Ensure proper storage, handling, and accountability of investigational products, if applicable.
  • Maintain regulatory documents and assist with IRB submissions.

Qualifications:

  • Bachelor's degree in a health-related field required.
  • At least 1–2 years of experience in clinical research preferred.
  • Phlebotomy certification or MA certification preferred.
  • Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
  • Excellent organizational skills and attention to detail.
  • Strong interpersonal and communication skills.
  • Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms).
  • Ability to work independently and as part of a multidisciplinary team.

Preferred Qualifications:

  • Experience working in clinical trials, especially in a hospital or academic setting.
  • Familiarity with IRB processes and clinical trial documentation.
  • Bilingual skills (depending on patient population) may be a plus.

Job Type: Full-time

Work Location: In person

Schedule:

  • 8 hour shift
  • Monday to Friday
  • Weekends as needed