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Medical Monitor Jobs (NOW HIRING)

AVEO Oncology

Medical Director

Boston, MA · On-site

... Monitoring and Safety Oversight: · Serve as the medical monitor for assigned clinical trials, providing ongoing medical oversight and guidance, addressing any issues that arise to ensure timely ...

Catholic Health

Monitor Technician

West Islip, NY · On-site

$26.86 - $34.86/hr

We are actively hiring Nursing Assistants to support our Emergency and Med-Surg units who are ready ... Monitor technician will place patient on cardiac monitor. This will require bending/lifting and ...

Catholic Health

Monitor Tech

Roslyn, NY

$25.23/hr

Assisting with the training of new staff in medical monitoring systems. * Technical will assist with the overall ED flow and provide excellent customer service to create a positive patient experience ...

Catholic Health

Monitor Tech

Roslyn, NY · On-site

$25.23/hr

Assisting with the training of new staff in medical monitoring systems. * Technical will assist with the overall ED flow and provide excellent customer service to create a positive patient experience ...

Umoja Biopharma

Senior Medical Director

Seattle, WA · On-site

$270K - $333K/yr

Serve as medical monitor for clinical studies, ensuring patient safety, data integrity, and compliance with GCP and regulatory requirements. * Lead preparation of clinical protocols, investigator ...

Umoja Biopharma

Senior Medical Director

Seattle, WA

$270K - $333K/yr

Serve as medical monitor for clinical studies, ensuring patient safety, data integrity, and compliance with GCP and regulatory requirements. * Lead preparation of clinical protocols, investigator ...

Catholic Health

Monitor Technician

West Islip, NY

$26.82 - $34.86/hr

Assisting with the training of new staff in medical monitoring systems. * Technician will assist with the overall ED flow and provide excellent customer service to create a positive patient ...

Catholic Health

Monitor Technician

West Islip, NY · On-site

$26.82 - $34.86/hr

Assisting with the training of new staff in medical monitoring systems. * Technician will assist with the overall ED flow and provide excellent customer service to create a positive patient ...

Catholic Health

Monitor Technician

West Islip, NY

$26.86 - $34.86/hr

We are actively hiring Nursing Assistants to support our Emergency and Med-Surg units who are ready ... Monitor technician will place patient on cardiac monitor. This will require bending/lifting and ...

Catholic Health

Monitor Tech

Roslyn, NY

$25.23/hr

Assisting with the training of new staff in medical monitoring systems. * Technical will assist with the overall ED flow and provide excellent customer service to create a positive patient experience ...

Alexion Pharmaceuticals

Provides medical leadership and mentorship to Medical Directors and Clinical Development Scientists; may serve as medical monitor. * Shapes therapeutic area and regulatory strategy; represents ...

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Medical Monitor information

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$21K

$92.6K

$178K

How much do medical monitor jobs pay per year?

As of Jun 15, 2026, the average yearly pay for medical monitor in the United States is $92,555.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,500.00 and $84,500.00 per year, depending on experience, location, and employer.

How much do medical monitors make in the US?

Medical monitors in the US typically earn an average salary ranging from $80,000 to $150,000 annually, depending on experience, location, and the complexity of clinical trials they oversee. They often hold certifications such as CCRP or CCRA and work in clinical research settings, with some roles offering additional compensation for on-call or travel duties.

What are the key skills and qualifications needed to thrive in the Medical Monitor position, and why are they important?

To thrive as a Medical Monitor, you need a deep understanding of clinical research, medical evaluation, and regulatory compliance, typically supported by a medical degree (MD or equivalent) and clinical experience. Familiarity with clinical trial management systems (CTMS), safety databases, and Good Clinical Practice (GCP) certification is essential. Excellent communication, analytical thinking, and problem-solving skills help you clearly communicate findings and collaborate with cross-functional teams. These competencies are vital to ensure participant safety, data integrity, and the smooth conduct of clinical trials.

What is a medical monitor job?

A medical monitor is a professional responsible for overseeing clinical trials to ensure participant safety, protocol compliance, and data integrity. They review adverse events, monitor site activities, and often hold certifications such as a clinical research associate (CRA) or medical license, working closely with investigators and sponsors throughout the trial process.

What is a Medical Monitor job?

A Medical Monitor is a physician responsible for ensuring the safety and integrity of clinical trials. They provide medical oversight by reviewing patient data, assessing adverse events, and ensuring compliance with regulatory guidelines. Medical Monitors work closely with clinical teams, investigators, and regulatory agencies to support the study's progress and ethical conduct. Their expertise helps ensure that trials meet safety standards while gathering reliable data for drug development.

What are the typical daily responsibilities of a Medical Monitor in a clinical research setting?

As a Medical Monitor, your daily responsibilities often include reviewing adverse event reports, monitoring patient safety data, and providing medical input during clinical trial meetings. You will interpret clinical data, ensure protocol adherence, and address any medical queries from site staff or sponsors. Additionally, you collaborate closely with clinical operations, safety, and regulatory teams to ensure trials are conducted safely and efficiently. This role requires ongoing communication with investigators and the ability to rapidly assess and respond to potential safety concerns.

What is the easiest medical job that pays well?

A medical monitor role typically requires knowledge of clinical trials and regulatory standards but often involves less direct patient care than other healthcare jobs. While it may require some specialized training or certification, it can offer a good salary with relatively manageable responsibilities compared to more demanding medical positions.

How much do medical monitors make?

Medical monitors in California typically earn between $80,000 and $150,000 annually, depending on experience, certifications, and the complexity of clinical trials they oversee. Salaries can vary based on the employer, location, and whether the role is full-time or contract-based, with some positions offering additional benefits such as health insurance and flexible schedules.
More about Medical Monitor jobs
What cities are hiring for Medical Monitor jobs? Cities with the most Medical Monitor job openings:
What are the most commonly searched types of Medical Monitor jobs? The most popular types of Medical Monitor jobs are:
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Medical Monitor jobs near you
Infographic showing various Medical Monitor job openings in the United States as of June 2026, with employment types broken down into 50% Part Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $92,555 per year, or $44.5 per hour.
Associate Medical Director, Clinical Development

Associate Medical Director, Clinical Development

Viridian Therapeutics, Inc.

Waltham, MA • On-site

$230K - $265K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago

Job description

Description
At Viridian, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team's expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic candidates for well-validated targets.
Reporting to the VP, Clinical Development, the Associate Medical Director, Clinical Development will support all aspects of clinical development (science and medical), including the generation and review of critical trial-related documents (e.g., investigator brochures, protocols, clinical study reports), contributing to regulatory submissions, and serving as the medical monitor for assigned studies.
This role can be fully remote or based in our Waltham, MA headquarters. Our office-based employees are required to work in the office three (3) days a week. If remote, travel to headquarters for meetings would be required at the discretion of management.
Responsibilities (including, but not limited to):
  • Assist Clinical Development Lead(s) on assigned clinical program/ trials
  • Support the development of clinical trial strategies, study designs and scientific strategy
  • Contribute to the clinical content of clinical and regulatory documents, including but not limited to protocols, INDs, CTAs, investigator brochures, CSR's; participate in review SAPs, TLF shells, emerging clinical trial data and data interpretation
  • Provide medical oversight as medical monitor on assigned trials and the Sponsor's medical representative to multiple vendors and collaborators
  • Contribute to preparation and interactions with regulatory authorities
  • Contribute to overall review of clinical data including data listings review in collaboration with Safety/PV, cross-functional teams and engaged vendors
  • Support activities associated with execution of clinical trials and data collection, including training of the internal team, vendors, and site staff; preparation of case report forms; review of protocol deviations; and resolution of issues
  • Partner closely with clinical operations, biostatistics, safety/PV, data management, program management, and research colleagues
  • Support management of DSMB activities
  • Stay current with GCP and worldwide regulatory requirements

Requirements
  • Requires a Medical Degree (MD or equivalent)
  • 3+ years relevant clinical development experience in the biotechnology or pharmaceutical industry; Immunology or Ophthalmology experience is a plus
  • Experience in multiple phases of clinical development desirable
  • Knowledge of FDA regulatory requirements, clinical research concepts & practices, and ICH/GCP guidelines
  • Ability for creative problem-solving, strategic thinking, risk identification & mitigation skills
  • Team-oriented and works collaboratively with cross-functional teams
  • Ability to demonstrate flexibility and adaptability in a dynamic environment
  • Experience working with and managing third party vendors, such as CRO's
  • Strong oral and written communication skills
  • Excellent interpersonal/ organizational skills with the ability to multi-task
  • Strong commitment to ethical standards
  • Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
  • Ability to travel up to 20%
  • The salary range for this position is commensurate with experience

Viridian offers a comprehensive benefits package including:
  • Competitive pay and stock options for all employees
  • Medical, dental, and vision coverage
  • Fertility and mental health programs
  • Short- and long-term disability coverage
  • Life, Travel and AD&D
  • 401(k) Company Match with immediate company vest
  • Employee Stock Purchase plan
  • Generous vacation plan and paid company holiday shutdowns
  • Various mental, financial, and proactive physical health programs covered by Viridian

Viridian Therapeutics, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination, harassment, or retaliation of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by Federal, State, and Local laws. Viridian will ensure that individuals with disabilities are provided 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. Please contact us to request accommodation.
Viridian Therapeutics, Inc participates in E-Verify, the federal program for electronic verification of employment eligibility.

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