$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 ...
$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 ...
$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 ...
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 ...
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 ...
Boston, MA · On-site
$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 ...
Boston, MA · On-site
$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 ...
Seattle, WA · On-site
$97.82 - $146.68/hr
The Clinical Research Monitor II supports the quality and regulatory compliance of investigator‑initiated oncology clinical trials conducted within the Cancer Consortium. This role performs remote ...
Seattle, WA · On-site
$97.82 - $146.68/hr
The Clinical Research Monitor II supports the quality and regulatory compliance of investigator‑initiated oncology clinical trials conducted within the Cancer Consortium. This role performs remote ...
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 ...
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 ...
Seattle, WA · Hybrid
$97K - $146K/yr
The Clinical Research Monitor II supports the quality and regulatory compliance of investigatorinitiated oncology clinical trials conducted within the Cancer Consortium. This role performs remote ...
Seattle, WA · Hybrid
$97K - $146K/yr
The Clinical Research Monitor II supports the quality and regulatory compliance of investigatorinitiated oncology clinical trials conducted within the Cancer Consortium. This role performs remote ...
Seattle, WA · Hybrid
$97K - $146K/yr
The Clinical Research Monitor II supports the quality and regulatory compliance of investigatorinitiated oncology clinical trials conducted within the Cancer Consortium. This role performs remote ...
Seattle, WA · Hybrid
$97K - $146K/yr
The Clinical Research Monitor II supports the quality and regulatory compliance of investigatorinitiated oncology clinical trials conducted within the Cancer Consortium. This role performs remote ...
Manhattan, NY · On-site
$90 - $120/hr
As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices Position Summary The Clinical research monitor, under the guidance of the Assistant ...
Manhattan, NY · On-site
$90 - $120/hr
As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices Position Summary The Clinical research monitor, under the guidance of the Assistant ...
Senior Clinical Research Monitor Location: Mounds View, MN Duration: 24+ (possibility of extension) MANDAOTORY REQUIRED 1) Device experience 2) Cardiovascular experience There is a total of 3 ...
Senior Clinical Research Monitor Location: Mounds View, MN Duration: 24+ (possibility of extension) MANDAOTORY REQUIRED 1) Device experience 2) Cardiovascular experience There is a total of 3 ...
The Clinical Research Monitoring Program is one of several investigator-initiated trial (IIT) specific support programs within KCCR. Function/Duties of Position OHSU Research classification
The Clinical Research Monitoring Program is one of several investigator-initiated trial (IIT) specific support programs within KCCR. Function/Duties of Position OHSU Research classification
Portland, OR · On-site
$90 - $120/hr
The Clinical Research Monitoring Program is one of several investigator-initiated trial (IIT) specific support programs within KCCR. Function/Duties of Position OHSU Research classification
Portland, OR · On-site
$90 - $120/hr
The Clinical Research Monitoring Program is one of several investigator-initiated trial (IIT) specific support programs within KCCR. Function/Duties of Position OHSU Research classification
Seattle, WA · On-site
$97K - $146K/yr
The Clinical Research Monitor II supports the quality and regulatory compliance of investigator-initiated oncology clinical trials conducted within the Cancer Consortium. This role performs remote ...
Seattle, WA · On-site
$97K - $146K/yr
The Clinical Research Monitor II supports the quality and regulatory compliance of investigator-initiated oncology clinical trials conducted within the Cancer Consortium. This role performs remote ...
The OCR Clinical Research Monitor II, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial ...
The OCR Clinical Research Monitor II, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial ...
The OCR Clinical Research Monitor II, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial ...
The OCR Clinical Research Monitor II, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial ...
The OCR Clinical Research Monitor II, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial ...
The OCR Clinical Research Monitor II, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial ...
$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 ...
$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 ...
Richmond, VA · On-site
$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 ...
Richmond, VA · On-site
$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 ...
The OCR Clinical Research Monitor II, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial ...
The OCR Clinical Research Monitor II, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial ...
The Clinical Trial Research Monitor is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and ...
The Clinical Trial Research Monitor is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and ...
As a Clinical Research Assistant/MA , you'll play a key role in supporting study visits ... Provide subject care, including explaining study procedures, answering questions, and monitoring ...
As a Clinical Research Assistant/MA , you'll play a key role in supporting study visits ... Provide subject care, including explaining study procedures, answering questions, and monitoring ...
$5.29 - $8.41
0% of jobs
$8.41 - $11.54
0% of jobs
$11.54 - $14.66
0% of jobs
$14.66 - $17.79
0% of jobs
$17.79 - $20.91
0% of jobs
$20.91 - $24.04
0% of jobs
$24.04 - $27.16
0% of jobs
$27.16 - $30.29
0% of jobs
$30.29 - $33.41
0% of jobs
$33.41 - $36.54
0% of jobs
$37.32 is the 25th percentile. Wages below this are outliers.
$36.54 - $39.66
100% of jobs
$5
$39
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.
| Aspect | Clinical Research Monitor | Clinical Research Associate |
|---|---|---|
| Certifications | Often required or preferred certifications like CCRP or CCRA | Similar certifications such as CCRP or CCRA are common |
| Work Environment | Monitoring visits at sites, reviewing data, ensuring compliance | Site visits, data collection, and regulatory documentation |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Pharmaceutical 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.
Cities with the most Clinical Research Monitor job openings:
The most popular types of Clinical Research Monitor jobs are:
The top employers for Clinical Research Monitor jobs are:
States with the most job openings for Clinical Research Monitor jobs include:
The top searched job categories for Clinical Research Monitor jobs are:
For Clinical Research Monitor jobs, the most frequently searched job titles are:

8.1
Based on 101 frontline employees who took The Breakroom Quiz
118th of 1,065 rated hospitals
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 SummaryConduct 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 FunctionsEducation 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 ConditionsThis 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 Statement0100 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 FrameworkAt 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.
Get the full story on Breakroom