How much does a Clinical Trials Specialist / Research Coordinator make in the United States?
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The average Clinical Trials Specialist / Research Coordinator salary in the United States is $66,861 as of July 01, 2026. The range for our most popular Clinical Trials Specialist / Research Coordinator positions (listed below) typically falls between $58,640 and $75,081. Keep in mind that salary ranges can vary widely depending on many important factors, including position, education, certifications, additional skills, and the number of years you have spent in your profession. With more online, real-time compensation data than any other website, Salary.com helps you determine your exact pay target.
Clinical Trials Specialist / Research Coordinator's Annual Base Salary
| Job Title | Salary | Hourly Rate | Location | Date Updated |
| clinical trials coordinator | $54,060 | $25.99 | United States | July 01, 2026 |
| Clinical Trials Research Director | $169,100 | $81.30 | United States | July 01, 2026 |
| Clinical Trials Research Manager | $118,280 | $56.87 | United States | July 01, 2026 |
| Clinical Trials Specialist | $59,178 | $28.45 | United States | July 01, 2026 |
| Clinical Trials Research Associate | $56,232 | $27.03 | United States | July 01, 2026 |
| Clinical Trials Regulatory Specialist | $64,696 | $31.10 | United States | July 01, 2026 |
| Clinical Trials Research Associate I | $69,800 | $33.56 | United States | July 01, 2026 |
| Clinical Trials Research Associate II | $82,000 | $39.42 | United States | July 01, 2026 |
| Clinical Trials Associate | $62,932 | $30.26 | United States | July 01, 2026 |
| Clinical Trials Manager | $109,675 | $52.73 | United States | July 01, 2026 |
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A clinical trials coordinator is responsible for overseeing the administration and management of clinical research studies. This role involves coordinating participant recruitment, ensuring compliance with regulatory requirements, and maintaining accurate documentation. The salary for a clinical trials coordinator typically ranges from $50,000 to $80,000 annually, depending on factors such as experience, education, and geographic location. Additional benefits may include health insurance, retirement plans, and opportunities for professional development. The position requires strong organizational skills, attention to detail, and the ability to communicate effectively with diverse stakeholders, including researchers, participants, and regulatory bodies. View clinical trials coordinator Salary
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The Clinical Trials Research Director oversees and ensures adherence to established processes and procedures, FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and JCAHO and International Conference on Harmonization (ICH) guidelines. Directs and oversees the team responsible for the design, administration, and execution of clinical research trials. Being a Clinical Trials Research Director may require an advanced degree. Designs, develops, and implements clinical processes, procedures, and programs. In addition, Clinical Trials Research Director may require ACRP or SOCRA certification. Typically reports to senior management. The Clinical Trials Research Director manages a departmental sub-function within a broader departmental function. Creates functional strategies and specific objectives for the sub-function and develops budgets/policies/procedures to support the functional infrastructure. Working as a Clinical Trials Research Director typically requires 5+ years of managerial experience. Deep knowledge of the managed sub-function and solid knowledge of the overall departmental function. View Clinical Trials Research Director SalaryAlternate Job Titles:Clinical Research Director, Clinical Research Programs Director
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The Clinical Trials Research Manager monitors and ensures adherence to established processes and procedures, FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and JCAHO and International Conference on Harmonization (ICH) guidelines. Manages the team responsible for the design, administration, and execution of clinical research trials. Being a Clinical Trials Research Manager may require a master's degree. May assist with the development and implementation of clinical processes, procedures, and programs. In addition, Clinical Trials Research Manager may require ACRP or SOCRA certification. Typically reports to a director. The Clinical Trials Research Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. Working as a Clinical Trials Research Manager typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes. View Clinical Trials Research Manager SalaryAlternate Job Titles:Clinical Research Manager, Clinical Research Programs Manager
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The Clinical Trials Research Associate I analyzes and evaluates clinical data gathered during research. Participates in the design, administration and monitoring of clinical trials. Being a Clinical Trials Research Associate I knowledge of FDA regulatory requirements is required. Ensures compliance with protocol and overall clinical objectives. In addition, Clinical Trials Research Associate I may require ACRP or SOCRA Clinical Research Professional exam completion. Requires a bachelor's degree in Science or its equivalent. Typically reports to a supervisor or manager. Being a Clinical Trials Research Associate I work is closely managed. Works on projects/matters of limited complexity in a support role. Working as a Clinical Trials Research Associate I typically requires 0-2 years of related experience. View Clinical Trials Research Associate I SalaryAlternate Job Titles:Clinical Research Associate I, Clinical Research Assistant I, Clinical Research Project Support Specialist I, Clinical Research Support Administrator I, Clinical Trials Data Analyst I
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The Clinical Trials Research Associate II analyzes and evaluates clinical data gathered during research. Participates in the design, administration and monitoring of clinical trials. Being a Clinical Trials Research Associate II knowledge of FDA regulatory requirements is required. Ensures compliance with protocol and overall clinical objectives. In addition, Clinical Trials Research Associate II may require ACRP or SOCRA Clinical Research Professional exam completion. Requires a master's degree in science or equivalent. Typically reports to a supervisor or manager. Being a Clinical Trials Research Associate II occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. Working as a Clinical Trials Research Associate II typically requires 2-4 years of related experience. View Clinical Trials Research Associate II SalaryAlternate Job Titles:Clinical Research Associate II, Clinical Research Assistant II, Clinical Research Project Support Specialist II, Clinical Research Support Administrator II, Clinical Trials Data Analyst II