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How much do clinical research professional jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for clinical research professional in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is a clinical research professional?

Clinical Research Professionals are specialists who design, conduct, monitor, and manage clinical trials that test the safety and effectiveness of medical treatments, drugs, and devices. They work in hospitals, research organizations, pharmaceutical companies, or academic institutions, ensuring that studies comply with regulatory requirements and ethical standards. Their roles may include coordinating trials, collecting and analyzing data, and ensuring the integrity and quality of research. Clinical Research Professionals play a crucial role in advancing medical knowledge and developing new therapies for patients.

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

To thrive as a Clinical Research Professional, you need a solid understanding of clinical trial protocols, regulatory compliance, and scientific methodology, typically supported by a degree in life sciences or a related field. Familiarity with clinical data management systems, Good Clinical Practice (GCP) certification, and regulatory submission tools is often required. Strong attention to detail, effective communication, and organizational skills help ensure successful study coordination and data integrity. These competencies are crucial for maintaining compliance, protecting patient safety, and producing credible research outcomes.

What are typical challenges faced by clinical research professionals when managing multiple studies simultaneously?

Clinical Research Professionals often juggle several studies at once, which can present challenges such as time management, ensuring compliance with regulatory requirements, and maintaining clear communication among diverse teams. Balancing the differing timelines, protocols, and stakeholder expectations for each study requires strong organizational skills and attention to detail. Many professionals find success by leveraging project management tools, setting clear priorities, and fostering collaborative relationships with study coordinators, investigators, and sponsors.

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

AspectClinical Research ProfessionalClinical Research Coordinator
CredentialsOften requires a degree in health sciences, life sciences, or related fields; certifications like CCRP are commonTypically holds a bachelor's degree in health sciences or related fields; certifications like CCRP may be preferred
Work EnvironmentWorks in research institutions, pharmaceutical companies, or CROs, overseeing multiple studiesWorks directly with study participants, managing daily activities at clinical sites
Employer & Industry UsageUsed across research organizations, pharma, and biotech companiesPrimarily employed at clinical trial sites, hospitals, or clinics

While both roles are integral to clinical research, the Clinical Research Professional typically has broader oversight and may handle multiple projects, whereas the Clinical Research Coordinator focuses on managing individual studies at the site level.

What career paths are in clinical research?

Career paths in clinical research include roles such as Clinical Research Coordinator, Clinical Data Manager, Clinical Research Associate, and Project Manager. These positions often require knowledge of Good Clinical Practice (GCP), regulatory guidelines, and experience with clinical trial management systems. Advancement can lead to senior roles, specialized positions, or management opportunities within pharmaceutical, biotech, or healthcare organizations.

What do clinical research professionals do?

Clinical research professionals design, manage, and oversee clinical trials to evaluate the safety and effectiveness of new medical treatments or devices. They coordinate with research teams, ensure compliance with regulatory standards, and collect and analyze data using specialized software. Strong organizational skills and knowledge of Good Clinical Practice (GCP) are essential for this role.
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Clinical Research Professional jobs near you
Infographic showing various Clinical Research Professional job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 20% Part Time, and 4% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $50,108 per year, or $24.1 per hour.

Clinical Research Professional I

Little Rock, AR • On-site

Arkansas Children's
Health Care and Social Assistance • 1 - 5K employees
Learn more about Arkansas Children'sexternal

$23 - $28.70/hr

Full-time

Posted 9 days ago

Arkansas Children's Hospital rating

7.5

Company rating: 7.5 out of 10

Based on 58 frontline employees who took The Breakroom Quiz

Job description

ARKANSAS CHILDREN'S IS A TOBACCO FREE WORKPLACE. FLU VACCINES ARE REQUIRED. ARKANSAS CHILDREN'S IS AN EQUAL OPPORTUNITY EMPLOYER. ALL QUALIFIED APPLICANTS WILL RECEIVE CONSIDERATION FOR EMPLOYMENT WITHOUT REGARD TO RACE, COLOR, RELIGION, SEX, SEXUAL ORIENTATION, GENDER IDENTITY OR EXPRESSION, NATIONAL ORIGIN, AGE, DISABILITY, PROTECTED VETERAN STATUS OR ANY OTHER CHARACTERISTIC PROTECTED BY FEDERAL, STATE, OR LOCAL LAWS.
This position has been designated as safety sensitive and cannot be filled by a candidate who is a current user of medical marijuana.
CURRENT EMPLOYEES: Please apply via the internal career site by logging into your Workday Account (https://www.myworkday.com/archildrens/)and search the "Find Jobs" report.
Work Shift:
Please see job description for details.
Time Type:
Full time
Department:
CC034460 Digital Biomarkers Smoking Cessation
Summary:
Salary:
Most new hires start between $23.00-$28.70 per hour, depending on experience and qualifications.
Additional Information:
The Clinical Research Professional I coordinates selected specific aspects of clinical research studies.
This role serves as a resource for research study participants, families, other healthcare providers, and members of the clinical research team regarding specified aspects of the study.
Required Education:
High school diploma or GED or equivalent
Recommended Education:
Bachelor's degree in a related field of study.
Required Work Experience:
High School Diploma/GED, or 2 years of experience in lieu of a diploma/GED.
Recommended Work Experience:
Required Certifications:
Recommended Certifications:
Certified Clinical Research Coordinator (CCRC) - Association of Clinical Research Professionals, Certified Clinical Research Professional (CCRP) - Society of Clinical Research Associates
Description
1. Recruits and screens patients for enrollment eligibility and participation in research projects. Obtains consent for participation in accordance with all government regulations and internal policies/procedures.
2. Prepares flowcharts, study specific source documents, and collects/records subject data on case report forms. Creates databases and performs date entry into the database.
3. Serves as a research resource to subjects, families, and other healthcare providers regarding the needs of study and subjects family preserving patient/subject privacy and maintaining confidentiality of subject information.
4. Promotes knowledge of current professional practice and research standards, laws and regulations that affect human subjects research.
5. Facilitates and improves collaboration with other departments to facilitate research across the continuum.
6. Coordinates/collects requested data for sponsor review during site visits. Assists study monitor(s) in chart and case report form review.
7. Maintains files and study documentation according to institutional and regulatory standards
8. The incumbent will participate in the smoking cessation intervention delivery. This will include training to become a quit coach and delivering quit coaching sessions to study participants.
9. This position will monitor incoming data to ensure a high level of quality. This will include monitoring data dashboards, as well as working with participants and collaborators to troubleshoot any data-related issues.
10. Performs other duties as assigned.

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