Clinical Research Associate Monitor Salary in Provo, UT
How Much Does a Clinical Research Associate Monitor make?
Clinical Research Associate Monitor made a median salary around $63,602 in March, 2025.
The best-paid 25 percent made $71,681 probably that year, while the lowest-paid 25 percent made around $55,897.
Salary ranges can vary widely depending on many important factors, including education, certifications, additional skills, 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.
Check out
Clinical Research Associate Monitor
jobs in
Provo, Utah
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Best-Paying Cities for Clinical Research Associate Monitor
The metropolitan areas that pay the highest salary in the Clinical Research Associate Monitor profession are Blanding
, Cisco
, La Sal
, Monticello
, Beryl
.
| Blanding, UT | $70,092 |
| Cisco, UT | $70,092 |
| La Sal, UT | $70,092 |
| Monticello, UT | $70,092 |
| Beryl, UT | $67,906 |
Best-Paying States for Clinical Research Associate Monitor
The states and districts that pay Clinical Research Associate Monitor the highest salary are District of Columbia (around $76,036)
, California (around $75,353)
, New Jersey (around $74,875)
, Alaska (around $74,396)
, and Massachusetts (around $74,328)
.
| District of Columbia | $76,036 |
| California | $75,353 |
| New Jersey | $74,875 |
| Alaska | $74,396 |
| Massachusetts | $74,328 |
What is the Career Path of Clinical Research Associate Monitor?
A career path is a sequence of jobs that leads to your short- and long-term career goals. Some follow a linear career path within one field, while others change fields periodically to achieve career or personal goals.
For Clinical Research Associate Monitor, the first career path typically starts with a Clinical Research Monitor II position , and then progresses to VP of Clinical Research Monitoring.
Additionally, the second career path typically starts with a Clinical Research Associate II position , and then progresses to VP of Clinical Research.
Besides, Clinical Research Associate Monitor can also turn to other related jobs, including
Clinical Research Monitor
,
Clinical Research Monitor I
,
Clinical Research Monitor II
and
Clinical Research Monitor III
.
Frequently Asked Questions for Clinical Research Associate Monitor
Q:
What is the salary range of Clinical Research Associate Monitor in Provo, UT?
A:
In 2025
, the lowest-paid Clinical Research Associate Monitor in Provo, UT earned an average annual salary of $55,897
, while the highest-paid made $71,681.
Q:
What is the salary for a Clinical Research Associate Monitor in California?
A:
Clinical Research Associate Monitor employed in California earned an average salary of $75,353 in 2025.
Average Clinical Research Associate Monitor Pay vs. Other Jobs
Clinical Research Associate Monitor earned an average salary of $63,602 in 2025.
Other jobs related to Clinical Research Associate Monitor earned the following average salary in March, 2025.
Clinical Research Monitor
made $63,602
,
Clinical Research Monitor I
made $81,290
,
Clinical Research Monitor II
and
Clinical Research Monitor III
made $95,685
and $120,098 respectively
.
Relevant Jobs of Clinical Research Associate Monitor
There is currently no job description for Clinical Research Monitor, be the first to
submit
the job responsibilities for Clinical Research Monitor.
Clinical Research Monitor I is responsible for monitoring clinical research trials across multiple study sites. Ensures all clinical research trials are conducted, recorded, and reported in adherence to established processes and procedures, FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and all other applicable regulatory requirements. Being a Clinical Research Monitor I verifies data collected is accurate and complete. May assist with design, development, and monitoring of clinical evaluation projects. Additionally, Clinical Research Monitor I requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. The Clinical Research Monitor I work is closely managed. Works on projects/matters of limited complexity in a support role. To be a Clinical Research Monitor I typically requires 0-2 years of related experience.
Clinical Research Monitor II is responsible for monitoring clinical research trials across multiple study sites. Ensures all clinical research trials are conducted, recorded, and reported in adherence to established processes and procedures, FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and all other applicable regulatory requirements. Being a Clinical Research Monitor II verifies data collected is accurate and complete. May assist with design, development, and monitoring of clinical evaluation projects. Additionally, Clinical Research Monitor II requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. The Clinical Research Monitor II occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. To be a Clinical Research Monitor II typically requires 2-4 years of related experience.
Clinical Research Monitor III is responsible for monitoring clinical research trials across multiple study sites. Ensures all clinical research trials are conducted, recorded, and reported in adherence to established processes and procedures, FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and all other applicable regulatory requirements. Being a Clinical Research Monitor III verifies data collected is accurate and complete. May assist with design, development, and monitoring of clinical evaluation projects. Additionally, Clinical Research Monitor III requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. The Clinical Research Monitor III work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Clinical Research Monitor III typically requires 4-7 years of related experience.
Clinical Research Monitor IV is responsible for monitoring clinical research trials across multiple study sites. Ensures all clinical research trials are conducted, recorded, and reported in adherence to established processes and procedures, FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and all other applicable regulatory requirements. Being a Clinical Research Monitor IV verifies data collected is accurate and complete. May assist with design, development, and monitoring of clinical evaluation projects. Additionally, Clinical Research Monitor IV requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. The Clinical Research Monitor IV work is highly independent. May assume a team lead role for the work group. A specialist on complex technical and business matters. To be a Clinical Research Monitor IV typically requires 7+ years of related experience.