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Clinical Research Associate Jobs in Park Ridge, IL

Clinical Research Associate - Cross Therapeutic Area - Chicago ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Our clinical philosophy Our approach to care is grounded in meeting patients where they are and ... About the Role As our first Research Associate, you will play a foundational role in building the ...

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Clinical Research Associate information

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$11

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$68

How much do clinical research associate jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for clinical research associate in Park Ridge, IL is $40.47, according to ZipRecruiter salary data. Most workers in this role earn between $28.37 and $51.78 per hour, depending on experience, location, and employer.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree such as a life sciences or healthcare-related field, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with clinical trial management systems can improve job prospects, but entry may be challenging for those without relevant qualifications or experience.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

What are the key skills and qualifications needed to thrive as a clinical research associate?

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and the chance to contribute to medical advancements, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in healthcare and research.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.
More about Clinical Research Associate jobs
What are the most commonly searched types of Clinical Research jobs in Park Ridge, IL? The most popular types of Clinical Research jobs in Park Ridge, IL are:
What job categories do people searching Clinical Research Associate jobs in Park Ridge, IL look for? The top searched job categories for Clinical Research Associate jobs in Park Ridge, IL are:
What cities near Park Ridge, IL are hiring for Clinical Research Associate jobs? Cities near Park Ridge, IL with the most Clinical Research Associate job openings:
Infographic showing various Clinical Research Associate job openings in Park Ridge, IL as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 19% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $84,174 per year, or $40.5 per hour.

Visiting Research Associate II - Medicine, Breathe Chicago Center

University of Illinois

Chicago, IL • On-site

$49K - $60K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 days ago


Job description

Visiting Research Associate II - Medicine, Breathe Chicago Center
Hiring Department:Department of Medicine
Location: Chicago, IL
Requisition ID:1042107
Posting Close Date: August 7, 2026
Salary: The budgeted salary range for the position is $49,000 to $60,000
About the University of Illinois Chicago
UIC is among the nation's preeminent urban public research universities, a Carnegie RU/VH research institution, and the largest university in Chicago. UIC serves over 34,000 students, comprising one of the most diverse student bodies in the nation and is designated as a Minority Serving Institution (MSI), an Asian American and Native American Pacific Islander Serving Institution (AANAPSI) and a Hispanic Serving Institution (HSI). Through its 16 colleges, UIC produces nationally and internationally recognized multidisciplinary academic programs in concert with civic, corporate and community partners worldwide, including a full complement of health sciences colleges. By emphasizing cutting-edge and transformational research along with a commitment to the success of all students, UIC embodies the dynamic, vibrant and engaged urban university. Recent "Best Colleges" rankings published by U.S. News & World Report, found UIC climbed up in its rankings among top public schools in the nation and among all national universities. UIC has over 300,000 alumni, and is one of the largest employers in the city of Chicago.
This position is intended to be eligible for benefits. This includes Health, Dental, Vision, Life Insurance, a Retirement Plan, Paid time Off, and Tuition waivers for employees and dependents.
Who We Are: The Breathe Chicago Center (BCC) in the Department of Medicine at the University of Illinois Chicago conducts research to identify new tests and treatments for people with chronic lung disease, COVID-19, Long COVID, and other conditions. We also use healthcare delivery science to increase access to high-quality healthcare. Studies are conducted in collaboration with academic health centers, community-based organizations, and faith-based organizations in Chicago and other cities across the nation.
General Job Summary: The Visiting Research Associate II conducts research by assisting with the collection and documentation of study data from research participants, cleaning of data, and other supportive functions to facilitate efficient teamwork in a clinical research environment.
This position may supervise junior staff. This position supports the implementation of effective strategies for optimizing the recruitment of research participants and for maintaining their active engagement through to the study's end. The incumbent works closely with management to ensure those study goals are met and that regulatory compliance is maintained. This position may be undertaken remotely/hybrid and will be focused on COVID-19 patient engagement by telephone.
Duties and Responsibilities:
• Perform surveys, interviews, observations, or use other methods according to established research protocols.
• Collect and review client evaluations/assessments, surveys, and participant interviews to develop reports for the PI and appropriate agencies and grant sponsors, allowing for evaluation of project implementation.
• May assist with study protocol development.
• Maintain compliance with established protocols, regulatory and monitoring agency standards, and grant sponsor guidelines.
• Assess patients for protocol eligibility and participation in clinical research.
• Participate in clinical research education and training programs.
• Execute informed consent process, ensuring willingness and understanding of the participant.
• Prepare and contribute statistical data and pertinent information for papers, grants, and other documents.
• Complete the required documentation for internal and external regulatory agencies.
• Schedule and conduct clinical research visits required by the protocol and track participant visits; may include completion of survey, interviews, or other protocol-specific testing.
• Perform other related duties and participate in special projects as assigned.
Minimum Requirements:
• Bachelor's degree in social science or related field required.
• A minimum of one year of related research experience.
• Knowledge of research concepts, practices, and procedures.
Preferred Qualifications
• Demonstrated ability to provide customer service involving work with patients, customers, and the general public.
• Proficiency in English and Spanish strongly preferred.
• Experience in a clinical research setting, experience working with federal regulations, and IRB's preferred.
• Familiarity with medical terminology and procedures.
• Ability to manage multiple tasks and deadlines. Ability to work in a flexible environment with shifting priorities.
• Demonstrated technology skills, including proficiency in Microsoft Office, REDCap, and EPIC.
• Excellent written and oral communication skills.
The University of Illinois System is an equal opportunity employer, including but not limited to disability and/or veteran status, and complies with all applicable state and federal employment mandates. Please visit Required Employment Notices and Posters to view our non-discrimination statement and find additional information about required background checks, sexual harassment/misconduct disclosures, and employment eligibility review through E-Verify.
The university provides accommodations to applicants and employees. Request an Accommodation
Artificial Intelligence (AI) tools may be used in some portions of the candidate review process for this position, however, all employment decisions will be made by a person.

University of Illinois logo

About University of Illinois

Sourced by ZipRecruiter

The University of Illinois, located in Urbana, Illinois, US, is a prominent entity in the higher education sector. Operating its official functions through its website uillinois.edu, the institution provides a range of educational programs and services. The University was founded in 1867 and has since grown dramatically both in size and reputation. Its core values are embodied in its mission to enhance the lives of its students and citizens in the state, nation, and world through leadership in learning, discovery, engagement, and economic development. The university boasts several notable achievements including producing Nobel laureates and Pulitzer prize winners. It is renowned for its research programs and is known for significant advancements across various fields including engineering, science, and humanities.

Industry

Colleges, universities, and professional schools

Company size

5,001 - 10,000 Employees

Headquarters location

Urbana, IL, US

Year founded

1974

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