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Clinical Research Assistant Jobs in Decatur, IL (NOW HIRING)

Certified Nurse Midwife - (Decatur)

Decatur, IL · On-site

$95K - $119K/yr

... clinical staff, nursing and medical assistant students. * Attend pertinent CME courses both within the School of Medicine and externally. RESEARCH * Assist the Obstetrics and Gynecology faculty in ...

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Clinical Research Assistant information

See Decatur, IL salary details

$7

$22

$44

How much do clinical research assistant jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for clinical research assistant in Decatur, IL is $22.03, according to ZipRecruiter salary data. Most workers in this role earn between $16.78 and $25.19 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 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 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 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 assistants often start with little or no experience, as entry-level positions may provide on-the-job training. Relevant skills such as attention to detail, basic knowledge of medical terminology, and familiarity with data entry or research protocols can help candidates qualify for these roles. Certifications like Good Clinical Practice (GCP) can also improve job prospects for those new to the field.
What are the most commonly searched types of Clinical Research jobs in Decatur, IL? The most popular types of Clinical Research jobs in Decatur, IL are:
What are popular job titles related to Clinical Research Assistant jobs in Decatur, IL? For Clinical Research Assistant jobs in Decatur, IL, the most frequently searched job titles are:
What job categories do people searching Clinical Research Assistant jobs in Decatur, IL look for? The top searched job categories for Clinical Research Assistant jobs in Decatur, IL are:
What cities near Decatur, IL are hiring for Clinical Research Assistant jobs? Cities near Decatur, IL with the most Clinical Research Assistant job openings:
Infographic showing various Clinical Research Assistant job openings in Decatur, IL as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $45,822 per year, or $22 per hour.

Phase 1 Clinical Research Assistant - EMT (Part-Time)

Accel Research Sites

Decatur, IL

Full-time, Part-time

Posted 16 days ago


Job description

Accel Research Sites in Decatur, GA, is seeking a part-time Research Assistant to support Clinical Research Coordinators and other site staff in compliance with regulations. Duties include assisting with patient enrollment and documentation, performing clinical tasks, and maintaining confidentiality. The ideal candidate will have necessary clinical qualifications and excellent communication skills to ensure effective teamwork. Opportunities for full-time benefits are available for those working 30 hours or more weekly. #J-18808-Ljbffr