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Clinical Research Assistant Jobs (NOW HIRING)

BioTalent

Clinical Research Assistant

Miami, FL

We are currently looking for a detail-oriented and motivated Clinical Research Assistant with experience supporting clinical research studies in compliance with FDA regulations, Good Clinical ...

New

Ohio State University

Clinical Research Assistant Department:Medicine | Psychiatry The university will not sponsor applicants for work visas for this position. This position requires traveling to research participants ...

Care Access

Clinical Research Assistant

Tyler, TX · On-site

How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while ...

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How much do clinical research assistant jobs pay per hour?

As of Jun 12, 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.

Can you be a CRA with no experience?

Becoming a Clinical Research Assistant (CRA) typically requires some knowledge of clinical trials, research protocols, and data management, but entry-level positions may be available to candidates with minimal experience if they demonstrate strong organizational skills and a willingness to learn. Many employers provide on-the-job training or require relevant certifications such as Good Clinical Practice (GCP). Having a background in healthcare, biology, or related fields can also improve chances of starting as a CRA without prior experience.

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.

How much does a CRC make?

A Clinical Research Coordinator (CRC) typically earns between $50,000 and $70,000 annually, depending on experience, education, and the complexity of clinical trials. Salaries can vary based on the employer, location, and certifications such as CCRP or CCRC, with some positions offering additional benefits or bonuses.

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.

Which is better, CRC or CRA?

A Clinical Research Coordinator (CRC) manages daily trial activities at research sites, while a Clinical Research Associate (CRA) monitors clinical trials remotely or on-site to ensure compliance and data quality. Both roles are essential in clinical research, with CRCs focusing on site operations and CRA roles emphasizing oversight and regulatory adherence; the choice depends on career interests and preferred work environment.

What do clinical research assistants do?

Clinical research assistants support the conduct of clinical trials by recruiting and screening participants, collecting and managing data, and ensuring compliance with study 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 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 June 2026, with employment types broken down into 1% As Needed, 77% Full Time, 21% Part Time, and 1% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $47,241 per year, or $22.7 per hour.

Clinical Research Assistant

Metro Infectious Disease Consultants

Decatur, GA

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 16 days ago

Job description

Metro Infusion Center/Metro Infectious Disease Consultants is seeking a Full-Time Clinical Research Assistant who will be responsible for providing non-clinical support in the operations and monitoring of clinical trials. The Research Assistant will analyze and evaluate clinical data gathered during research while ensuring compliance with protocols and overall clinical objectives. Responsibilities assigned to individuals can and will change at any time at the discretion of management or the supervisor

Schedule: Monday-Friday 8:30am-5:00 pm, in-person

Duties:

  • Enter data proficiently and accurately into a data capture system for sponsors and contract research organizations to monitor.
  • Request or acquire the equipment and supplies necessary for each project.
  • Set up, calibrate, and maintain laboratory and/or field research equipment, as specified by the requirements of the study.
  • Assist Clinical Research Associates that are monitoring each study (on and off-site).
  • Invoice for payments associated with the clinical trial budget.
  • Ship lab samples while following regulations and protocols when needed.
  • Attend project meetings and communicate with fellow staff through email and phone calls.
  • Perform ECG's
  • Upload study documents to EMR chart
  • Track specimen shipments
  • Responsibilities may evolve depending on protocol specific requirements

Requirements

  • High school diploma required
  • Bachelor's Degree preferred
  • Proof of current vaccinations, including recommended boosters, commonly required for those working with immunocompromised patients, including measles, mumps, rubella, varicella, hepatitis A & B, influenza.

Requests for accommodations/exceptions will be considered on a case-by-case basis, consistent with applicable laws.

Benefits

  • 401(k)
  • Dental insurance
  • Health insurance
  • Life insurance
  • Paid time off
  • Referral program
  • Vision insurance
  • $50,000-$53,000 ($20/hour + monthly bonus)

Apply