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Clinical Research Associate Bridge Program Jobs in Illinois

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 ...

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 ...

Senior Clinical Research Associate - Cardiovascular Device - Central/West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

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 ...

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 ...

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 ...

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 Bridge Program information

See Illinois salary details

$11

$39

$67

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

As of Sep 7, 2026, the average hourly pay for clinical research associate bridge program in Illinois is $39.85, according to ZipRecruiter salary data. Most workers in this role earn between $27.93 and $51.01 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.

What are popular job titles related to Clinical Research Associate Bridge Program jobs in Illinois?

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

What job categories do people searching Clinical Research Associate Bridge Program jobs in Illinois look for?

The top searched job categories for Clinical Research Associate Bridge Program jobs in Illinois are:

What cities in Illinois are hiring for Clinical Research Associate Bridge Program jobs?

Cities in Illinois with the most Clinical Research Associate Bridge Program job openings:

Infographic showing various Clinical Research Associate Bridge Program job openings in Illinois as of August 2026, with employment types broken down into 86% Full Time, and 14% Temporary. Highlights an 100% In-person job distribution, with an average salary of $82,892 per year, or $39.9 per hour.

Clinical Research Associate, Cardiology

Northwestern University

Evanston, IL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

New


Northwestern University rating

7.5

Company rating: 7.5 out of 10

Based on 49 frontline employees who took The Breakroom Quiz

316th of 631 rated colleges and universities


Job description

Department: MED-Cardiology
Salary/Grade: RES/
Job Summary:
The Division of Cardiology is seeking a full-time Clinical Research Associate for an exciting, expanded role in cutting-edge research in heart failure and heart transplantation. This position is 100% supported by funding from federal and non-profit organizations, under the supervision of Dr. Palak Shah
The Clinical Research Associate role will be responsible for managing research-related activities for multicenter clinical trials in adult and pediatric heart transplantation. Under direction of the PI, assists in performing biomedical research. This may involve recruiting subjects for studies, preparation and submission of IRB regulatory materials, preparation and submission of OSR documents, administering tests &/or questionnaires; collecting, compiling, tabulating &/or processing responses; gathering information; &/or assisting in the preparation of material for inclusion in reports.The candidate will need to ensure that all study activities are completed by strictly following Good Clinical Practices (GCP) and all current local, state, and federal laws, regulations, guidance, policy & procedure developed by the Northwestern University Institutional Review Board (IRB), Food and Drug Administration (FDA) Code of Federal Regulations (CFR), and the International Conference on Harmonization (ICH).
This hybrid position is located on the Northwestern University Chicago Campus with one day per week remote or flexible hours. Please include a cover letter detailing relevant experience and interest with clinical research.
Please note:
Working environment may include an ambulatory clinic &/or hospital setting.
Specific Responsibilities:
  • Recruits research subjects for clinical studies; provides list to check in area of subjects who will be coming in that day; may bring subjects into exam rooms; Provides all necessary support during studies. May administer informed consent.
  • Assists PI and other investigators in preparation and submission of IRB regulatory materials, preparation and submission of OSR documents (including consent forms), maintenance of records according to all regulations.
  • Assists research coordinator in collecting, compiling, tabulating &/or processing responses; gathering information; &/or assisting in the preparation of material for inclusion in reports and journals. Assists with submission to journals.
  • Assists with processing subject reimbursement materials
  • Assists PI with other mandatory regulatory and compliance areas such as CT.Gov
Miscellaneous
Performs other duties as assigned.
Minimum Qualifications:
  • Ability to successfully complete the requirements of the Northwestern Memorial Hospital Research Access Program.
  • Master's degree or higher
Minimum Competencies: (Skills, knowledge, and abilities.)
  • Excellent interpersonal skills
  • Ability to multitask
  • Technologically proficient
  • Critical Thinking Skills
  • Effective written and oral communicator
Preferred Qualifications:
  • Project Management Certification
  • Doctoral degree (PhD)
  • Previous experience in both observational and interventional clinical research
  • CITI, GCP, HIPAA training
Preferred Competencies: (Skills, knowledge, and abilities)
  • Advanced medical terminology
  • Familiarity with IRB and clinical trial regulatory requirements
  • Familiarity with electronic medical record systems
  • Basic specimen processing skills
  • Familiarity with invoicing and study financial tracking
Benefits:
At Northwestern, we are proud to provide meaningful and competitive benefits. The available benefits package for this position will include health, dental, vision, disability, and life insurance; paid vacation and holidays; paid medical/sick and parental leave; tuition benefits for the employee and dependents; pre-tax and flex spending accounts for commuting and dependent care; generous retirement savings options; and wellness programs. For a comprehensive overview of available benefits, including eligibility details, visit us at https://www.northwestern.edu/hr/benefits/index.html to learn more.
Work-Life and Wellness:
Northwestern offers comprehensive programs and services to help you and your family navigate life's challenges and opportunities, and adopt and maintain healthy lifestyles.
We support flexible work arrangements where possible and programs to help you locate and pay for quality, affordable childcare and senior/adult care. Visit us at https://www.northwestern.edu/hr/benefits/work-life/index.html to learn more.
Professional Growth & Development:
Northwestern supports employee career development in all circumstances whether your workspace is on campus or at home. If you're interested in developing your professional potential or continuing your formal education, we offer a variety of tools and resources. Visit us at https://www.northwestern.edu/hr/learning/index.html to learn more
Northwestern University is an Equal Opportunity Employer and does not discriminate on the basis of protected characteristics, including disability and veteran status. View Northwestern's non-discrimination statement . Job applicants who wish to request an accommodation in the application or hiring process should contact the Office of Civil Rights and Title IX Compliance. View additional information on the accommodations process .

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