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Clinical Research Assistant Jobs in Park Ridge, IL

University Retina

Clinical Research Assistant

Lemont, IL · On-site

$21 - $23.50/hr

Position Summary We are now hiring for a Clinical Research Assistant that will support a high-volume Resarch Department within an ophthalmic practice that focuses on providing quality and ...

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Clinical Research Assistant information

See Park Ridge, IL salary details

$8

$22

$45

How much do clinical research assistant jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical research assistant in Park Ridge, IL is $22.35, according to ZipRecruiter salary data. Most workers in this role earn between $17.02 and $25.53 per hour, depending on experience, location, and employer.

What is a clinical research assistant?

Clinical Research Assistants are professionals who support clinical research studies by performing a range of administrative and research-related tasks. They help collect and manage data, assist with patient recruitment, prepare study materials, and ensure compliance with research protocols and regulations. Their work is crucial in advancing medical knowledge and ensuring that clinical trials run smoothly and ethically. Clinical Research Assistants often work under the supervision of principal investigators or clinical research coordinators in hospitals, universities, or pharmaceutical companies.

What does a clinical research assistant do?

A clinical research assistant—or clinical research associate (CRA)—helps lead researchers during clinical trials for new drugs and medical devices. As a clinical research assistant, your responsibilities include preparing the laboratory, processing volunteers, taking biological samples or vital signs, and organizing data. You may also be required to set up and clean work areas. Your job is to assist the researchers in any way possible, helping them conduct sound, ethical, and scientifically accurate research.

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

To thrive as a Clinical Research Assistant, you need a bachelor’s degree in a life science or health-related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and good clinical practice (GCP) certification are typically required. Excellent communication, teamwork, and problem-solving abilities help you excel in coordinating with research teams and participants. These skills ensure accurate data collection, regulatory compliance, and the smooth execution of clinical studies.

What are some common challenges clinical research assistants face when coordinating multiple studies simultaneously?

Clinical Research Assistants often manage several studies at once, which can lead to challenges in balancing competing deadlines, maintaining accurate documentation, and ensuring compliance with complex protocols. Effective time management and organizational skills are crucial to handle overlapping tasks such as scheduling patient visits, collecting data, and preparing regulatory submissions. Collaborating closely with principal investigators, coordinators, and other team members helps distribute the workload and maintain research quality. Developing strong communication habits and utilizing digital tracking tools can further streamline workflow and reduce errors.

What is the difference between Clinical Research Assistant vs Clinical Research Coordinator?

AspectClinical Research AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCRC are common
Work EnvironmentAssists in data collection, patient scheduling, and administrative tasks in clinical trial settingsManages study protocols, patient recruitment, and regulatory compliance in clinical trial sites
Employer & IndustryHospitals, research institutions, pharmaceutical companiesHospitals, research centers, pharmaceutical companies

Both roles support clinical research but differ in responsibilities. Clinical Research Assistants focus on data collection and administrative tasks, while Clinical Research Coordinators oversee study management and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.

Can you be a clinical research assistant with no experience?

Clinical research assistant positions often require some knowledge of medical terminology and data management, but many entry-level roles are available for candidates without prior experience. Employers may provide on-the-job training and look for strong organizational skills, attention to detail, and the ability to follow protocols. Certifications such as Good Clinical Practice (GCP) can enhance prospects for those new to the field.
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Clinical Research Assistant jobs near you
Infographic showing various Clinical Research Assistant job openings in Park Ridge, IL as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 19% Part Time, 6% Contract, and 1% Nights. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $46,485 per year, or $22.3 per hour.

Clinical Research Assistant

Cardiovascular Associates of America

Schaumburg, IL • On-site

Full-time

Posted 10 days ago

Job description

Clinical Research Assistant
This will be an in-person position in Schaumburg
Position Summary
The Clinical Research Assistant (CRA) provides operational and participant support for clinical research studies conducted at the site. This position assists Clinical Research Coordinators (CRCs), investigators, and study teams with participant scheduling, specimen processing, investigational product accountability support, supply management, and study-related documentation.
The Clinical Research Assistant plays a critical role in ensuring efficient study conduct while allowing coordinators to focus on protocol management, participant care, and study execution.
Essential Responsibilities
Participant Support and Scheduling
  • Coordinate participant appointments and study visits.
  • Contact participants regarding upcoming visits and study requirements.
  • Assist with visit preparation and participant flow.
  • Maintain study calendars and visit schedules.
  • Support participant retention activities.

Study Operations
  • Maintain research supplies and study materials.
  • Order study-related supplies and equipment as directed.
  • Monitor inventory levels and maintain adequate stock.
  • Track expiration dates of study supplies and research materials.
  • Ensure study materials are organized and readily available.

Specimen Processing and Shipping
  • Process biological specimens according to protocol requirements.
  • Prepare and package specimens for shipment.
  • Complete shipping documentation and laboratory requisitions.
  • Maintain specimen shipment records.
  • Coordinate with central laboratories and couriers.

Study Documentation and Logs
  • Maintain temperature logs and equipment monitoring records.
  • Maintain medication accountability logs and inventory documentation.
  • Assist with essential study documentation.
  • Ensure logs are completed, accurate, and up to date.
  • Support filing and organization of study records.

Regulatory and Administrative Support
  • Assist with document collection and filing.
  • Route study documents for review and signature.
  • Support maintenance of regulatory binders and electronic regulatory systems.
  • Assist with study start-up and close-out activities.

Quality and Compliance
  • Follow protocol requirements, GCP, sponsor requirements, and site SOPs.
  • Escalate protocol deviations, equipment issues, or documentation concerns.
  • Participate in training and quality improvement activities.
  • Maintain confidentiality of participant and study information.

Qualifications
Education
  • High School Diploma required.
  • Associate's or Bachelor's degree in a health science, biological science, or related field preferred.

Experience
  • Current or previous Pharmacy Technician experience is required
  • Experience handling specimens or laboratory procedures preferred.

Knowledge, Skills, and Abilities
  • Strong organizational skills.
  • Ability to manage multiple priorities.
  • Attention to detail and accuracy.
  • Strong communication and customer service skills.
  • Ability to work independently and within a team environment.
  • Proficiency with Microsoft Office applications.
  • Ability to learn CTMS, EDC, and sponsor systems.

Physical Requirements
  • Ability to stand, walk, and move throughout clinical areas.
  • Ability to lift and transport study supplies and specimen shipments up to 25 pounds.
  • Ability to perform repetitive computer-based tasks.

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