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Clinical Research Associate Bridge Program Jobs in Chicago, IL

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Senior Clinical Research Associate

Chicago, IL · Hybrid

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Chicago ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

ICON

Senior Clinical Research Associate

Chicago, IL · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Chicago ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

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Clinical Research Associate

Chicago, IL

Clinical Research Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

Alira Health

Clinical Research Associate

Geneva, IL · On-site

Summary ROLE The Clinical Research Associate is an important member of the Alira Health Clinical ... DESIRED QUALIFICATION & EXPERIENCE * BS/BA from an undergraduate program or equivalent experience ...

ICON

Senior Clinical Research Associate

Chicago, IL · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Midwest ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

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Senior Clinical Research Associate

Chicago, IL · On-site

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Midwest ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

ICON

Clinical Research Associate 2

Chicago, IL · On-site +1

$91K - $114K/yr

Clinical Research Associate- Mid-West ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...

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Clinical Research Associate 2

Chicago, IL · On-site

$91K - $114K/yr

Clinical Research Associate- Mid-West ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...

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All JobsClinical Research Associate Bridge Program JobsClinical Research Associate Bridge Program Jobs in Chicago, IL

Clinical Research Associate Bridge Program information

See Chicago, IL salary details

$12

$42

$71

How much do clinical research associate bridge program jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for clinical research associate bridge program in Chicago, IL is $42.37, according to ZipRecruiter salary data. Most workers in this role earn between $29.71 and $54.23 per hour, depending on experience, location, and employer.

What is a Clinical Research Associate Bridge Program?

A Clinical Research Associate (CRA) Bridge Program is a specialized training course designed to help individuals transition into the role of a CRA, especially those with related experience in healthcare, life sciences, or clinical research support. These programs typically combine classroom instruction with practical training, focusing on topics such as clinical trial monitoring, regulatory compliance, and Good Clinical Practice (GCP) guidelines. The goal is to equip participants with the necessary knowledge and skills to begin a career as a CRA, often including job placement assistance or internships. Bridge programs are ideal for those who want to move into clinical research from a related field but lack direct CRA experience.

What types of mentorship and training can I expect in a Clinical Research Associate Bridge Program?

Participants in a Clinical Research Associate (CRA) Bridge Program typically receive structured mentorship from experienced CRAs and clinical research professionals. The program often includes hands-on training in protocol review, site monitoring, regulatory compliance, and data management, combined with classroom or online learning modules. You'll work closely with cross-functional teams, such as clinical project managers and regulatory specialists, gaining exposure to industry-standard processes and tools. This supportive environment is designed to accelerate your transition into a CRA role and help you build a strong professional network within clinical research.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate in a bridge program?

To thrive as a Clinical Research Associate in a bridge program, you need a foundational understanding of clinical trials, regulatory compliance, and data management, usually supported by a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Strong attention to detail, effective communication, and organizational skills help you manage study protocols and collaborate with diverse teams. These competencies are crucial for ensuring clinical trial integrity, regulatory adherence, and the successful execution of research studies.

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For Clinical Research Associate Bridge Program jobs in Chicago, IL, the most frequently searched job titles are:

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The top searched job categories for Clinical Research Associate Bridge Program jobs in Chicago, IL are:

What cities near Chicago, IL are hiring for Clinical Research Associate Bridge Program jobs?

Cities near Chicago, IL with the most Clinical Research Associate Bridge Program job openings:

Clinical Research Associate Bridge Program jobs near you
Infographic showing various Clinical Research Associate Bridge Program job openings in Chicago, IL as of June 2026, with employment types broken down into 2% As Needed, 74% Full Time, 20% Part Time, 2% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $88,121 per year, or $42.4 per hour.

Clinical Research Associate

Medasource

North Chicago, IL • On-site

Other

Posted 10 days ago

Job description

Title: Clinical Research Associate

Duration: 1 year contract (potential of extension)

Location: Remote with up to 75% travel


Job Description:

Abbott's Core Diagnostics team is seeking a Clinical Research Associate to support a Traumatic Brain Injury (TBI) clinical research initiative. This individual will support multi-site clinical trial operations while ensuring strict compliance with protocol in a highly regulated environment. The ideal candidate brings strong monitoring fundamentals, exceptional attention to detail, and the ability to operate independently across multiple sites and stakeholders.


Responsibilities:

  • Perform site qualification, initiation, interim monitoring, and close-out visits across assigned clinical sites
  • Support oversight of approximately 4-5 clinical research sites, including primary and secondary site responsibilities
  • Ensure protocol compliance, GCP adherence, and accurate study documentation
  • Conduct source data verification/review and investigational product accountability activities
  • Identify, document, and escalate site issues, deviations, and risks appropriately
  • Complete detailed trip reports, monitoring documentation, and required reporting within established timelines
  • Collaborate cross-functionally with clinical operations, investigators, and study coordinators
  • Support multiple studies simultaneously as needed
  • Maintain compliance with time tracking, reporting, and data handling procedures

Qualifications:

  • 3-5+ years of clinical research experience preferred
  • Open to candidates with:
  • CRA experience within sponsor environments
  • Strong clinical research coordinator experience from hospital or academic settings
  • Strong understanding of:
  • Site monitoring activities
  • Source data verification/review
  • Investigational product accountability
  • GCP and clinical trial documentation requirements
  • Excellent written and verbal communication skills
  • Strong critical thinking and situational problem-solving abilities
  • Ability to work independently and manage competing priorities across multiple sites
  • Highly organized with strong time management skills
  • Ability to travel nationally up to 75% as required
  • Comfortable operating within a 40-hour work week structure


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