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Clinical Research Monitor Jobs (NOW HIRING)

$51 - $82/hr

... 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 ...

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 ...

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 ...

$70 - $80/hr

FDA program Administrator/Clinical Research Monitor Responsibilities: * Perform risk-based monitoring * Develop monitoring plans for new sponsor-investigator clinical trials and studies that get ...

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Clinical Research Monitor information

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How much do clinical research monitor jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical research monitor in the United States is $38.70, according to ZipRecruiter salary data. Most workers in this role earn between $38.22 and $39.18 per hour, depending on experience, location, and employer.

What is a clinical research monitor?

A clinical research monitor, also called a clinical research associate, oversees the operations of a clinical trial to ensure that it meets all safety and governmental regulations. As a clinical research monitor, your job duties include traveling to testing sites, inspecting the procedures, documenting results from the trial, and verifying that all collected data is accurate and verified. Your primary responsibility is to make sure the testing is conducted safely and within industry and governmental guidelines.

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

To thrive as a Clinical Research Monitor, you need a solid understanding of clinical trial protocols, regulatory compliance (such as GCP), and a degree in life sciences or a related field. Familiarity with electronic data capture systems, trial management software, and certifications like ACRP or SOCRA are highly valued. Excellent organizational skills, attention to detail, and effective communication are essential soft skills for managing site relationships and ensuring protocol adherence. These competencies are crucial for safeguarding data integrity, patient safety, and regulatory compliance throughout the clinical trial process.

What are some common challenges clinical research monitors face when overseeing multiple study sites?

Clinical Research Monitors often encounter challenges such as managing varying levels of compliance across different sites, coordinating communication between site staff and sponsors, and ensuring timely data collection and reporting. Travel between sites and adapting to diverse protocols or site-specific processes can also present logistical hurdles. Successful monitors develop strong organizational skills, maintain meticulous documentation, and build collaborative relationships with site teams to navigate these challenges effectively.

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

AspectClinical Research MonitorClinical Research Associate
CertificationsOften required or preferred certifications like CCRP or CCRASimilar certifications such as CCRP or CCRA are common
Work EnvironmentMonitoring visits at sites, reviewing data, ensuring complianceSite visits, data collection, and regulatory documentation
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms

Both roles involve overseeing clinical trial activities, ensuring compliance, and maintaining data integrity. While the titles are often used interchangeably, the term 'Clinical Research Monitor' emphasizes the monitoring aspect, whereas 'Clinical Research Associate' may encompass broader responsibilities in clinical trial management. Both roles require similar certifications and work in comparable environments within the industry.

What does a clinical research monitor do in clinical research?

A clinical research monitor oversees the progress of clinical trials to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. They conduct site visits, review data for accuracy, and verify that trial procedures are followed correctly, often using electronic data capture systems. Monitoring is essential for maintaining data integrity and participant safety throughout the study.

What cities are hiring for Clinical Research Monitor jobs?

Cities with the most Clinical Research Monitor job openings:

What are the most commonly searched types of Clinical Research Monitor jobs?

The most popular types of Clinical Research Monitor jobs are:

Who are the top companies hiring for Clinical Research Monitor jobs?

The top employers for Clinical Research Monitor jobs are:

What states have the most Clinical Research Monitor jobs?

States with the most job openings for Clinical Research Monitor jobs include:

Infographic showing various Clinical Research Monitor job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $80,500 per year, or $38.7 per hour.

$51 - $82/hr

Other

Posted 5 days ago


Brigham and Women's Hospital rating

8.1

Company rating: 8.1 out of 10

Based on 101 frontline employees who took The Breakroom Quiz

118th of 1,065 rated hospitals


Job description

Site: Mass General Brigham Incorporated

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.

Job Summary

Conduct site monitoring visits in accordance with standards of practice guidelines and federal regulations to ensure that the rights and well-being of human subjects are protected and electronic case report forms (e-CRF) are accurate, complete, and verifiable from source documents.

Essential Functions
  • Responsible for conducting study monitoring visits to assess protocol and regulatory compliance per the approved monitoring plan.
  • Review and compare source documentation to CRFs to ensure data is complete and accurate.
  • Draft site monitoring plans
  • Provide Investigator and study staff training at study initiation and as needed through the course of the trial
  • Review study-specific site documents, including regulatory documents, drug and device accountability logs, training logs, and delegation of authority logs.
  • Maintain regular communication with assigned sites to support site enrollment, data entry, query resolution, and patient retention.
  • Document site visit findings and observations via trip reports and letters.
  • Escalate major visit findings as described in the monitoring plan to appropriate study team members.
  • Prepare trip reports and follow-up letters; track issues to closure via CAPA where needed
  • Participate in weekly meetings with the study team.
Qualifications

Education Bachelor's Degree required; experience can be considered in lieu of a degree

Experience 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 member. Strong attention to detail and organizational skills. Knowledge of clinical research protocols. Knowledge of data management programs. Computer literacy. Knowledge of clinical trials, research, and general medicine.

Additional Job Details (if applicable)Working Conditions

This is a hybrid role that requires an on-site presence at the office (325 Cambridge Street in Boston) 3x/week This is a full-time position with a Monday through Friday schedule during standard Eastern Time business hours Remote workdays require a stable, secure, quiet, and HIPAA‑compliant workspace. This will be confirmed via Microsoft Teams video for all employees

Remote Type Hybrid Work Location 325 Cambridge Street Scheduled Weekly Hours 40 Employee Type Regular Work Shift Day (United States of America) Pay Range $50,502,40 - $82,014,40/Annual Grade 6

At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package.

In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth.

EEO Statement

0100 Mass General Brigham Incorporated is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran’s Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at (857)-282-7642.

Mass General Brigham Competency Framework

At Mass General Brigham, our competency framework defines what effective leadership “looks like” by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People‑Focused, half Performance‑Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.

Combat disease. Hold a hand. Help people. Impact the world.

Mass General Brigham is a passionate, welcoming community where minds meet caring hearts. Come be a part of the world’s most powerful force in medicine, where every role is important in changing lives. Are you ready? Our history includes New England hospitals founded over 200 years ago, some of the first and most prestigious hospitals in the world. Built on the legacy of two leading academic medical centers, we’re more than a system—we’re leaders in the practice of medicine. Mass General Brigham is committed to serving the community. We are dedicated to enhancing patient care, teaching and research, and taking a leadership role as an integrated health care system. We recognize that increasing value and continuously improving quality are essential to maintaining excellence.

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