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How much do clinical research assistant jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for clinical research assistant in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What are Clinical Research Assistants?

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.

Is CRC an entry level position?

A Clinical Research Assistant (CRA) is often considered an entry-level position in clinical research, suitable for individuals with a bachelor's degree in a related field. The role typically involves supporting study coordination, data collection, and regulatory documentation, with some positions requiring prior internship or related experience. Advancement may require additional certifications or experience in clinical trial management or specific therapeutic areas.

What are the key skills and qualifications needed to thrive as a Clinical Research Assistant, and why are they important?

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 qualifications do I need to be a clinical research assistant?

A clinical research assistant typically needs a bachelor's degree in health sciences, biology, or a related field. Relevant skills include attention to detail, organizational abilities, and familiarity with clinical trial protocols and data management tools. Some positions may require certification such as the Certified Clinical Research Professional (CCRP).

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.

How much money do clinical research assistants make?

Clinical research assistants typically earn a median annual salary of around $45,000 to $55,000, depending on experience, location, and the complexity of the research environment. Entry-level positions may start lower, while those with specialized skills or certifications can earn higher wages.

What do clinical research assistants do?

Clinical research assistants support the conduct of clinical trials by collecting and managing data, preparing study materials, and ensuring compliance with protocols and regulations. They often work under the supervision of investigators and may use electronic data capture systems, requiring attention to detail and knowledge of Good Clinical Practice (GCP) guidelines.
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Clinical Research Assistant jobs near you
Infographic showing various Clinical Research Assistant job openings in the United States as of July 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution, with an average salary of $47,241 per year, or $22.7 per hour.
Clinical Research Assistant

Clinical Research Assistant

University Physicians' Association

Knoxville, TN

Other

Posted 13 days ago

Job description

Description

University Physicians' Association, Inc. is seeking a qualified full-time Clinical Research Assistant candidate for Edmunds Gastroenterology, a fast-paced GI practice in Knoxville, TN. 


Job Summary

The Clinical Research Assistant supports the planning, coordination, and execution of clinical research studies in compliance with regulatory requirements, study protocols, and institutional policies. This role assists investigators and clinical research staff with participant recruitment, data collection, documentation, and study-related administrative tasks to ensure high-quality and ethical research conduct.


Key Responsibilities:

  • Assist with the day-to-day operations of clinical research studies and trials
  • Support participant recruitment, screening, enrollment, and follow-up activities
  • Collect, record, and maintain accurate study data in case report forms (CRFs), electronic data capture systems, and source documents
  • Prepare and maintain regulatory binders and study documentation in accordance with IRB, GCP, and sponsor requirements
  • Coordinate study visits, schedules, and communications with participants and study staff
  • Assist with informed consent processes under the supervision of authorized personnel
  • Perform basic clinical tasks as permitted (e.g., vital signs, specimen handling, questionnaire administration)
  • Able to do lab draws on patients
  • Support monitoring visits, audits, and inspections
  • Ensure confidentiality and proper handling of protected health information (PHI)
  • Communicate effectively with investigators, coordinators, sponsors, and regulatory bodies
  • Assist with inventory management of study supplies and investigational products (as applicable)

Requirements

Required:

  • Strong attention to detail and organizational skills
  • Ability to follow protocols, standard operating procedures, and regulatory guidelines
  • Proficiency with Microsoft Office and basic data management tools
  • Excellent written and verbal communication skills
  • Phlebotomy Experience 

Preferred:

  • Prior experience in clinical research, healthcare, or laboratory settings
  • Familiarity with Good Clinical Practice (GCP) and IRB processes

Skills and Competencies:

  • Strong time management and multitasking abilities
  • Professional and ethical conduct
  • Ability to work independently and as part of a multidisciplinary team
  • Problem-solving and critical-thinking skills
  • Comfort interacting with patients and research participants

Work Environment:

  • Clinical, hospital, academic, or research office setting
  • May involve direct patient interaction
  • Possible early mornings, occasional evenings, or weekend hours depending on study requirements

Physical Requirements:

  • Ability to sit, stand, and walk for extended periods
  • Ability to lift and move light research materials and supplies

Apply