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Clinical Research Monitor Jobs (NOW HIRING)

Clinical Research Monitor We are seeking a highly skilled Clinical Research Monitor to independently manage monitoring activities and support Phase I and Phase II clinical research studies. The role ...

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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 ...

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Clinical Research Monitor information

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How much do clinical research monitor jobs pay per hour?

As of Jul 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, and why are they important?

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 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 are Clinical Research Monitors?

Clinical Research Monitors, also known as Clinical Research Associates (CRAs), are professionals responsible for overseeing clinical trials to ensure they comply with regulatory requirements, study protocols, and ethical standards. They act as a link between the trial sponsor and research sites, monitoring data integrity, participant safety, and proper documentation. Their work helps ensure that clinical studies are conducted ethically and that results are valid and reliable.

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 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 June 2026, with employment types broken down into 3% As Needed, 75% Full Time, 19% Part Time, and 3% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $80,500 per year, or $38.7 per hour.
Clinical Research Monitor

Clinical Research Monitor

Actalent

New Haven, CT

$70 - $80/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Be an early applicant


Job description

Job Title: Clinical Research Monitor
Job Description

We are seeking a highly skilled Clinical Research Monitor to independently manage monitoring activities and support Phase I and Phase II clinical research studies. The role involves reviewing study documentation, source records, regulatory files, and trial data to ensure protocol compliance and adherence to Good Clinical Practice (GCP).

Responsibilities

  • Conduct independent monitoring activities for clinical trials.
  • Support Phase I and Phase II clinical research studies.
  • Review study documentation, source records, regulatory files, and trial data.
  • Ensure protocol compliance and adherence to GCP.
  • Schedule monitoring visits and prepare monitoring visit reports.
  • Draft confirmation and follow-up letters.
  • Follow up with sites to resolve action items.
  • Resolve Electronic Data Capture (EDC) queries.
Essential Skills
  • 3+ years of clinical research monitoring experience.
  • Experience in independent monitoring.
  • Experience with Phase I and/or Phase II clinical trials.
  • Proficiency in EDC and Trial Master File (TMF) systems.
Additional Skills & Qualifications
  • Background in neuroscience or neurology.
  • Experience in imaging research.
  • Familiarity with academic research environments.
Work Environment

The position offers a flexible schedule with approximately 8–10 monitoring visits per quarter. Onsite visits typically last 6–8 hours, while remote visits last 4–6 hours. Advance notice is provided for required visits. The role is based within the Institute for Neurodegenerative Disorders (IND), a premier clinical and imaging research facility focused on developing innovative neuroimaging tools and evaluating new treatments.

Job Type & Location

This is a Contract position based out of New Haven, CT.

Pay and Benefits

The pay range for this position is $70.00 - $80.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in New Haven,CT.

Application Deadline

This position is anticipated to close on Jul 14, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

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