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How much do clinical researcher jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical researcher in the United States is $30.97, according to ZipRecruiter salary data. Most workers in this role earn between $28.12 and $37.02 per hour, depending on experience, location, and employer.

What is a clinical researcher?

A clinical researcher works with a team of microbiologists, lab technicians, and other medical science professionals in order to work on new medicines and treatments for the health care industry. In this role, Your duties include conducting trials for medical research, in which you analyze the effects of drugs or treatments on study groups and control groups to compare their effects. A control group is a research group that has no exposure to treatment. You may also be responsible for writing up reports to present to sponsors. A clinical researcher must follow and practice all the rules of ethical scientific research.

What are some common challenges faced by clinical researchers when managing multiple studies simultaneously?

Clinical researchers often juggle several studies at once, which can present challenges such as balancing strict timelines, ensuring regulatory compliance, and maintaining accurate documentation for each project. Coordination with multidisciplinary teams—including physicians, statisticians, and regulatory specialists—can also add complexity to daily tasks. Effective time management, clear communication, and strong organizational skills are essential for successfully handling competing priorities and delivering high-quality research outcomes.

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

AspectClinical ResearcherClinical Research Coordinator
Required CredentialsBachelor's or higher in life sciences; often advanced degreesTypically bachelor's degree in health sciences or related field
Work EnvironmentResearch institutions, pharmaceutical companies, universitiesHospitals, clinics, research sites
Employer & Industry UsageInvolved in designing and analyzing studiesManages daily study operations and participant coordination
Common Search & Comparison IntentUnderstanding research roles and responsibilitiesLearning about study coordination and participant management

While both roles are essential in clinical research, Clinical Researchers focus on designing and analyzing studies, often requiring advanced degrees. Clinical Research Coordinators handle the day-to-day management of clinical trials, working closely with participants and study sites. Understanding these differences helps in choosing the right career path or job role within the industry.

Do clinical researchers make good money?

Clinical researchers typically earn a median salary that varies by experience, education, and location, with many earning between $60,000 and $100,000 annually. Those with advanced degrees, certifications, or specialized skills in data analysis and regulatory compliance tend to earn higher salaries, especially in larger organizations or pharmaceutical companies.

What do you do as a clinical researcher?

A clinical researcher designs and conducts studies to evaluate the safety and effectiveness of medical treatments, drugs, or devices. They collect and analyze data, follow regulatory guidelines, and often work in hospitals, research institutions, or pharmaceutical companies, requiring strong analytical skills and knowledge of clinical trial protocols.

What qualifications do you need to be a clinical researcher?

To become a clinical researcher, a bachelor's degree in a health-related field such as biology, nursing, or medicine is typically required, with many roles preferring or requiring a master's or doctoral degree. Relevant skills include knowledge of clinical trial protocols, data analysis, and regulatory requirements, along with certifications like Good Clinical Practice (GCP) training. Experience in healthcare or research settings is also valuable.
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Clinical Researcher jobs near you
Infographic showing various Clinical Researcher job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $64,418 per year, or $31 per hour.

Clinical Research Coordinator

FIDES clinical research

Sandy Springs, GA • On-site

$24 - $32/hr

Other

This job post has expired 2 days ago. Applications are no longer accepted.

Job description

Company Description FIDES Clinical Research is a dedicated clinical research organization focused on conducting high-quality clinical trials that advance medical knowledge and improve patient care. The team collaborates with sponsors, healthcare professionals, and participants to ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards. FIDES Clinical Research emphasizes data integrity, participant safety, and clear communication throughout the research process. The organization offers a professional environment where clinical research staff can develop their skills and contribute meaningfully to the progress of new therapies and treatments.
Role Description This is a full-time, on-site Clinical Research Coordinator role based in Sandy Springs, GA. The Clinical Research Coordinator will manage day-to-day study activities, including screening and enrolling participants, scheduling study visits, and maintaining accurate source documentation and case report forms. Responsibilities include coordinating informed consent discussions, ensuring adherence to study protocols, handling regulatory submissions, and maintaining study files. The role involves close collaboration with investigators, sponsors, monitors, and site staff to ensure compliance with Good Clinical Practice (GCP) and institutional policies. The coordinator will also track study timelines, report adverse events, and support data entry, query resolution, and overall study quality.
Qualifications
  • Experience with informed consent processes and participant education, ensuring ethical and compliant enrollment.
  • Strong understanding of study protocols and ability to implement protocol requirements accurately in daily study operations.
  • Solid research skills, including data collection, documentation, and use of electronic data capture systems.
  • Demonstrated clinical research experience, preferably in coordinating clinical trials in outpatient or site-based settings.
  • Familiarity with clinical trials conduct, Good Clinical Practice (GCP), and regulatory guidelines (FDA, IRB).
  • Excellent organizational skills, attention to detail, and ability to manage multiple studies or tasks simultaneously.
  • Effective written and verbal communication skills for interacting with participants, investigators, monitors, and sponsors.
  • Ability to work on-site in Sandy Springs, GA, and collaborate within a multidisciplinary clinical research team.
  • Proficiency in basic computer applications and electronic medical record (EMR) or clinical trial management systems is beneficial.
  • Associate or bachelor’s degree in a health-related field, life sciences, or equivalent experience in clinical research is preferred.

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