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Clinical Research Associate Monitor Salary in New Mexico

How Much Does a Clinical Research Associate Monitor make?

Clinical Research Associate Monitor made a median salary around $63,358 in April, 2025. The best-paid 25 percent made $71,407 probably that year, while the lowest-paid 25 percent made around $55,683. 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.
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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 Capulin , Des Moines , Folsom , Raton , Santa Fe .
Capulin, NM $65,520
Des Moines, NM $65,520
Folsom, NM $65,520
Raton, NM $65,520
Santa Fe, NM $64,644

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 $75,740) , California (around $75,452) , Massachusetts (around $74,447) , Washington (around $74,173) , and New Jersey (around $74,146) .
District of Columbia $75,740
California $75,452
Massachusetts $74,447
Washington $74,173
New Jersey $74,146

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 New Mexico?
A: In 2025 , the lowest-paid Clinical Research Associate Monitor in New Mexico earned an average annual salary of $55,683 , while the highest-paid made $71,407.
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 $75,452 in 2025.

Average Clinical Research Associate Monitor Pay vs. Other Jobs

Clinical Research Associate Monitor earned an average salary of $63,358 in 2025. Other jobs related to Clinical Research Associate Monitor earned the following average salary in April, 2025. Clinical Research Monitor made $63,358 , Clinical Research Monitor I made $57,565 , Clinical Research Monitor II and Clinical Research Monitor III made $71,674 and $85,568 respectively .

Relevant Jobs of Clinical Research Associate Monitor

Clinical Research Monitor - Average Salary $63,358
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 - Average Salary $57,565
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. Verifies data collected is accurate and complete. May assist with design, development, and monitoring of clinical evaluation projects. Requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Work is closely managed. Works on projects/matters of limited complexity in a support role. Typically requires 0-2 years of related experience.
Clinical Research Monitor II - Average Salary $71,674
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. Verifies data collected is accurate and complete. May assist with design, development, and monitoring of clinical evaluation projects. Requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. Typically requires 2-4 years of related experience.
Clinical Research Monitor III - Average Salary $85,568
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. Verifies data collected is accurate and complete. May assist with design, development, and monitoring of clinical evaluation projects. Requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. Typically requires 4-7 years of related experience.
Clinical Research Monitor IV - Average Salary $104,371
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. Verifies data collected is accurate and complete. May assist with design, development, and monitoring of clinical evaluation projects. Requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Work is highly independent. May assume a team lead role for the work group. A specialist on complex technical and business matters. Typically requires 7+ years of related experience.
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