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Clinical Monitor Jobs (NOW HIRING)

Hrcrs

The Clinical Monitor is primarily responsible for monitoring and validating clinical trial data, ensuring data quality, integrity, and compliance with regulatory requirements. This individual will ...

Luminate Medical

In-House Clinical Monitor

New York, NY · On-site

We're looking for an In-House Clinical Monitor to play a key role in ensuring the quality, compliance, and successful execution of our clinical trials. Working closely with our Director of Clinical ...

Luminate Medical

In-House Clinical Monitor

In-House Clinical Monitor Opportunity at Luminate Luminate is on a mission to change the way we experience cancer care. We design and build products which revolutionize the patient experience of ...

Vrtx

Clinical Monitoring Associate Director

Boston, MA · On-site +1

$157K - $235K/yr

... monitor and evaluate Clinical Research Associate (CRA) and Lead CRA workloads and liaise with the Clinical Monitoring management team to ensure appropriate allocation of resources and optimal ...

New

Vertex Pharmaceuticals LLC

$157K - $235K/yr

... monitor and evaluate Clinical Research Associate (CRA) and Lead CRA workloads and liaise with the Clinical Monitoring management team to ensure appropriate allocation of resources and optimal ...

New

Actalent

Clinical Research Monitor

Philadelphia, PA · Remote

Clinical Research Monitor This fully remote Clinical Research Monitor role focuses on supporting IND‑regulated clinical trials within an academic research environment. The position centers on risk ...

New

Mass General Brigham

Clinical Research Monitor

Boston, MA · On-site

$50K - $82K/yr

At least 1-2 years of clinical research experience required * Previous experience with monitoring highly preferred Knowledge, Skills, and Abilities * Ability to work independently and as a team ...

Dana-Farber Cancer Institute

The Clinical Trials Monitor helps to ensure compliance of the clinical research enterprise with all related regulatory policies and guidelines, including federal, state, local, as well as the ...

Massgeneralbrigham

Clinical Research Monitor

Boston, MA · On-site

$50K - $82K/yr

At least 1-2 years of clinical research experience required * Previous experience with monitoring highly preferred Knowledge, Skills, and Abilities * Ability to work independently and as a team ...

Mass General Brigham Incorporated

... clinical research experience required Previous experience with monitoring highly preferred Knowledge, Skills, and Abilities Ability to work independently and as a team member. Strong attention to ...

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Clinical Monitor information

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$14

$34

$90

How much do clinical monitor jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical monitor in the United States is $34.62, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $32.93 per hour, depending on experience, location, and employer.

What is a clinical monitor?

A Clinical Monitor, also known as a Clinical Research Associate (CRA), is a professional responsible for overseeing clinical trials to ensure they are conducted in compliance with regulatory requirements and study protocols. They act as a liaison between the study sponsor and the clinical site, monitoring data quality, ensuring participant safety, and verifying that proper procedures are followed. Clinical Monitors regularly visit trial sites to review documentation, address issues, and provide training or guidance to site staff. Their work is essential for maintaining the integrity of clinical research and ensuring that results are accurate and reliable.

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

To thrive as a Clinical Monitor, you need a solid background in life sciences or a related field, along with knowledge of clinical research protocols and regulations such as GCP (Good Clinical Practice). Familiarity with electronic data capture (EDC) systems, clinical trial management software, and often a certification like ACRP or SOCRA is highly valued. Attention to detail, strong organizational skills, and effective communication are essential soft skills that distinguish top performers. These competencies ensure trials are conducted ethically, data integrity is maintained, and regulatory compliance is achieved for successful study outcomes.

What are the typical challenges faced by clinical monitors when overseeing multiple clinical trial sites?

Clinical Monitors often face the challenge of managing several trial sites simultaneously, which requires strong organizational and communication skills. They must ensure each site adheres to study protocols, regulatory requirements, and data quality standards, often while troubleshooting site-specific issues remotely. Balancing frequent travel, site visits, and documentation responsibilities can be demanding, making time management and adaptability essential for success in this role.

What is the difference between Clinical Monitor vs Clinical Research Associate?

AspectClinical MonitorClinical Research Associate
CertificationsOften required: CCRA, RAC, or similar certificationsOften required: CCRA, RAC, or similar certifications
Work EnvironmentMonitoring clinical trial sites, ensuring complianceOverseeing trial progress, data collection, and site management
Employer & Industry UsagePharmaceutical, biotech, CROsPharmaceutical, biotech, CROs

Both Clinical Monitors and Clinical Research Associates play vital roles in clinical trials, often sharing certifications and working within similar environments. The main difference lies in their focus: Clinical Monitors primarily oversee site compliance and conduct on-site visits, while Clinical Research Associates may have broader responsibilities including data management and trial coordination. Both roles are essential for successful clinical research and are frequently used interchangeably in the industry.

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Clinical Monitor jobs near you
Infographic showing various Clinical Monitor 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 $72,002 per year, or $34.6 per hour.

Clinical Monitor

On-site

Hrcrs
See more jobs at Hrcrsexternal

Other

Posted 4 days ago

Job description

The Clinical Monitor is primarily responsible for monitoring and validating clinical trial data, ensuring data quality, integrity, and compliance with regulatory requirements. This individual will work closely with the data management team and other stakeholders to facilitate accurate data collection and processing.

QUALIFICATIONS:
  • Bachelor’s degree in a life science, data science, or related field. However, a combination of experience and/or education will be taken into consideration.
  • Minimum of 2 years of experience in clinical monitoring or data management within a Contract Research Organization (CRO), biotech, or pharmaceutical company.
  • Understanding of GCP, FDA, and other regulatory requirements related to clinical monitoring.
  • Excellent attention to detail and problem-solving skills.
  • Good communication and interpersonal skills.
  • Proficiency in clinical monitoring software and other relevant tools.
KEY RESPONSIBILITIES:
  • Monitor and validate clinical trial data for accuracy, consistency, and completeness.
  • Ensure compliance with data management and monitoring procedures, standards, and regulatory guidelines.
  • Collaborate with data management and clinical trial teams to facilitate accurate and timely data collection and processing.
  • Identify and resolve data discrepancies or issues in a timely manner.
  • Participate in data audits and support the preparation of the clinical trial data for audits and inspections.
  • Maintain up-to-date knowledge of regulatory requirements related to clinical monitoring.
  • Assist in the development of clinical monitoring processes, standards, and training materials.
  • Performs other duties as assigned.
LOCATION AND TRAVEL REQUIREMENTS:

This is a fully remote position and may be performed anywhere within the United States of America. Occasional domestic and international travel may be required for company meetings, site visits, audits, etc.

This Company participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

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