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Medical Monitor Jobs (NOW HIRING)

Everest Clinical Research

Medical Director

$200K - $275K/yr

Acting as the primary Medical Monitor for assigned studies, the Medical Director serves as a key medical point of contact for investigative sites and sponsors, providing real-time medical guidance ...

Everest Clinical Research

Senior Medical Director

$250K - $325K/yr

Acting as the primary Medical Monitor for assigned studies, the Senior Medical Director serves as a key medical point of contact for investigative sites and sponsors, providing real-time medical ...

The Emmes Company, LLC

Medical Officer

Rockville, MD · Remote

Cooperates directly with Safety Monitors, Project Leadership, Data Managers and other relevant functional groups. * At the project level, will function in the role of a Medical Monitor leading the ...

Syneoshealth

OR · On-site

Provides medical oversight of assigned clinical studies in the duty as a medical monitor. Often serves as primary medical contact for customers for assigned clinical studies. * Provides medical input ...

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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 12, 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.
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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.
Medical Monitor

Medical Monitor

Artech Information System LLC

Lawrence Township, NJ

Contractor

Posted 26 days ago

Job description

Company Description

Artech is the 10th Largest ITStaffing Company in the US, according to Staffing Industry Analysts' 2012annual report. Artech provides technical expertise to fill gaps in clients'immediate skill-sets availability, deliver emerging technology skill-sets,refresh existing skill base, allow for flexibility in project planning andexecution phases, and provide budgeting/financial flexibility by offeringcontingent labor as a variable cost. 

Job Description

Job Description

  • Clinical Trial Medical Monitor

Role Imperatives

  • Work with Clinical Trial Lead/Program Lead or Early Asset Development Lead and cross functional study team to monitor and clean ongoing oncology studies, and support database locks.
  • Work with the clinical team to review the safety data using different tools: J-Review, CIOMS and CFR imaging tools.

Essential Core Behaviors

  • Ability to work and communicate efficiently with internal partners
  • Working effectively in a matrix organization
  • Ability to work independently

Desired Background, Knowledge, And Experience

  • MD or DO with experience in Oncology
  • A minimum of 3 - 5 years of industry experience
  • In depth knowledge of and experience as a medical monitor for clinical trials (Phase I - III)
  • Good verbal and written communication skills essential
  • Experience managing projects in a matrix environment, coordinating activities and adhering to tight timelines
  • Excellent written and verbal communication skills are required
  • Attend weekly update meeting with BMS core team (PM, DM, stats, CRO) as required
  • Respond to site and Health Authority questions about the protocol
  • Weekly investigator calls for Phase I studies as needed
  • Monthly review of Jreview and CRO data listings and QNET lab data. Attend monthly safety meetings
  • Review daily lab alerts and SAEs. Communicate with CRO sites regarding follow-up.
  • Monthly review of protocol deviations
  • Attend and present at Investigator meetings
  • CRF review
  • Present study updates as needed
  • Design and implement safety monitoring plans
  • DBL (final listing review, review of blinded TLF, review protocol deviations, participate in all DBL meetings)
  • CSR writing (review final TLFs, work with medical writer to review & revise CSR document, draft discussion and conclusions, participate in comment resolution meetings)
  • Topline results presentation
  • Other tasks may be required as determined during the project by BMS
  • The position is preferably based in the Princeton, NJ area but working remotely with occasional face to face meeting acceptable depending on business needs. Will need to be present in NJ for initial onboarding/training.
Qualifications
  • MD or DO with experience in Oncology
  • A minimum of 3 - 5 years of industry experience
Additional Information

All your information will be kept confidential according to EEO guidelines.

Artech logo

About Artech

Sourced by ZipRecruiter

Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).

Industry

Recruiting and staffing services

Company size

10,000+ Employees

Headquarters location

Morristown, NJ, US

Year founded

1992

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