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Remote Medical Monitor Clinical Trial Jobs (NOW HIRING)

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... remote patient monitoring and any/all decentralized trial processes * Tracks, monitors and reports ...

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

Clinicia Expert - Remote

Seattle, WA · Remote

$150 - $200/hr

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

Clinicia Expert - Remote

Washington, DC · Remote

$150 - $200/hr

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

Clinicia Expert - Remote

San Jose, CA · Remote

$150 - $200/hr

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

Clinicia Expert - Remote

Boston, MA · Remote

$150 - $200/hr

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

Clinicia Expert - Remote

Chicago, IL · Remote

$150 - $200/hr

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

Clinicia Expert - Remote

Miami, FL · Remote

$150 - $200/hr

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

Clinicia Expert - Remote

Boston, MA · Remote

$150 - $200/hr

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

Clinicia Expert - Remote

Austin, TX · Remote

$150 - $200/hr

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

Clinicia Expert - Remote

Boston, MA · Remote

$150 - $200/hr

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

Clinicia Expert - Remote

Los Angeles, CA · Remote

$150 - $200/hr

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

Clinicia Expert - Remote

Boston, MA · Remote

$150 - $200/hr

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

Clinicia Expert - Remote

Houston, TX · Remote

$150 - $200/hr

... clinical content, reviewing trial data, and providing expert medical judgment. No prior AI ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

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Remote Medical Monitor Clinical Trial information

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How much do remote medical monitor clinical trial jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for remote medical monitor clinical trial in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What is the difference between Remote Medical Monitor Clinical Trial vs Remote Clinical Research Coordinator?

AspectRemote Medical Monitor Clinical TrialRemote Clinical Research Coordinator
CredentialsMedical degree or clinical background, certifications like CCRP or CCRA often preferredBachelor's degree, often in health or science fields; certifications like CCRP beneficial
Work EnvironmentPrimarily remote, overseeing trial safety and complianceRemote or on-site, managing study logistics and participant coordination
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch institutions, hospitals, CROs

The Remote Medical Monitor Clinical Trial focuses on overseeing patient safety and trial compliance remotely, often requiring clinical credentials. In contrast, the Remote Clinical Research Coordinator manages study logistics and participant coordination, with a broader range of educational backgrounds. Both roles are essential in clinical research but differ in responsibilities and required qualifications.

More about Remote Medical Monitor Clinical Trial jobs

What cities are hiring for Remote Medical Monitor Clinical Trial jobs?

Cities with the most Remote Medical Monitor Clinical Trial job openings:

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

The most popular types of Medical Monitor Clinical Trial jobs are:

What states have the most Remote Medical Monitor Clinical Trial jobs?

States with the most job openings for Remote Medical Monitor Clinical Trial jobs include:

Infographic showing various Remote Medical Monitor Clinical Trial job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Full-time

Posted 4 days ago


Job description

The Clinical Trial Manager (CTM) is responsible for managing the clinical and operational activities of assigned clinical studies. This is accomplished by ensuring all projects are completed on-time and on-budget while following all company policies, Standard Operating Procedures (SOPs) and applicable regulatory guidelines. Plan, develop, and follow systems and procedures to ensure optimum compliance in accordance with GCP/ICH guidelines and FDA regulations. Ensure operating quality and efficiency.
Essential Duties and Responsibilities
  • Support or lead clinical study activities from start-up through closeout, ensuring adherence to timelines, budget, quality standards, SOPs, and regulatory requirements.
  • Oversee development and maintenance of study documentation including informed consent forms, IRB submissions, project plans, tracking tools, financial worksheets, and regulatory files.
  • Engage with investigative sites during start-up to coordinate CDAs, feasibility assessments, budgets, and CTAs.
  • Manage and maintain the Trial Master File (TMF), ensuring accuracy, completeness, and inspection readiness.
  • Oversee monitoring activities, including review and approval of monitoring visit reports, tracking site issues, data queries, protocol deviations, and ensuring timely resolution.
  • Assign, mentor, and support CRAs; lead team training, provide performance feedback, and ensure ongoing staff compliance with required training.
  • Monitor enrollment trends, operational risks, and study metrics; develop mitigation strategies and escalate issues appropriately.
  • Conduct internal team calls, participate in Sponsor meetings, and serve as key contact for site, CRA, and Sponsor inquiries.
  • Coordinate clinical resource planning, monitoring schedules, and budget oversight related to monitoring activities; support PM with grant administration and invoicing.
  • Participate in development/testing of clinical systems and process improvement initiatives.
  • Perform co‑monitoring visits and, when needed, assume CRA responsibilities.
  • Complete vendor reconciliation and support cross-functional collaboration to ensure data quality.

Qualifications
  • Bachelor's degree or RN in a related field or equivalent combination of education, training and experience
  • Supervisory experience preferred
  • Minimum 3 years' experience in clinical research industry
  • Minimum of 2 years' experience as a Clinical Monitor/Clinical Research Associate (CRA) strongly preferred
  • Working knowledge of GCPs, ICH guidelines, FDA and other applicable regulations
  • Specialized knowledge of CNS therapeutic areas
  • Proficiency in Microsoft Word, Excel, Powerpoint and Outlook
  • Proficiency with Teams and Zoom
  • Effective writing and verbal skills, English language
  • Meticulous attention to detail
  • Time management and ability to prioritize
  • Ability to travel 10-20%

Department Clinical Operations Role Clinical Trial Manager Locations Remote, US Remote status Fully Remote Employment type Full-time