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Medical Monitor Jobs (NOW HIRING)

Worldwide Clinical Trials Holdings, Inc.

NY · On-site

$134.50 - $267.50/hr

Role Overview The Medical Director, Medical Affairs provides medical management and professional medical support for clinical research projects as the assigned Medical Monitor (MM). Responsibilities

The Emmes Company, LLC

Medical Officer

Rockville, MD · On-site

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 ...

Taiho Oncology

$323K - $381K/yr

This position serves as a responsible medical monitor or a Lead medical monitor for various clinical phase 1 - 3 trials, as needed. Uses medical/scientific expertise to create or support the creation ...

Emmes

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 ...

IQVIA

Medical Director, Neurologist

Durham, NC · Remote

$154K - $431K/yr

Medical Monitoring: * Primarily serves as Medical Monitor (at the global or regional level) on assigned clinical trials. * Serves as Scientific Advisor (providing medical advice and input) to Project ...

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Medical Monitor information

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$21K

$92.6K

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How much do medical monitor jobs pay per year?

As of Jul 23, 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 salaries increasing with years of experience and specialized skills.

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.

How much does a medical monitor make?

The average salary for a medical monitor in Maryland ranges from $80,000 to $130,000 annually, depending on experience, certifications, and the employer. Medical monitors typically oversee clinical trial safety and compliance, often requiring knowledge of Good Clinical Practice (GCP) and relevant regulatory guidelines.

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.

How to become a clinical monitor?

To become a clinical monitor, typically one needs a bachelor's degree in a health-related field, such as nursing, pharmacy, or life sciences. Gaining experience in clinical research or healthcare and obtaining certifications like the Certified Clinical Research Professional (CCRP) can enhance prospects. Strong attention to detail, knowledge of Good Clinical Practice (GCP), and familiarity with clinical trial management systems are also important.

What is the role of a medical monitor?

A medical monitor oversees clinical trials to ensure participant safety, compliance with protocols, and data integrity. They review adverse events, monitor patient progress, and collaborate with investigators, often requiring medical licensure and knowledge of regulatory guidelines.

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.

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 July 2026, with employment types broken down into 1% As Needed, 78% Full Time, 14% Part Time, and 7% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $92,555 per year, or $44.5 per hour.

Medical Monitor (US Board-Certified Gastroenterologist)

PSI CRO

Remote

Full-time

Posted 16 days ago

Job description

Company Description

PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being.

Home-Based in United States

Responsibilities:

  • Acts as the primary point of contact for all parties on all trial-specific medical and safety-related questions
  • Provides input for responses to regulatory authorities and Institutional Review Boards (IRBs)/Independent Ethics Committees (IECs) on trial-specific medical and safety-related questions
  • Monitors trial participant safety
  • Participates in trial participant recruitment boost and retention activities
  • Presents on medical matters at kick-off and investigator meetings
  • Trains trial team in the therapeutic area and medical aspects of the protocol
  • Develops and reviews trial-specific documents within the scope of medical monitoring
  • Manages ongoing trial risks related to medical monitoring
  • Performs ongoing medical review of the operational clinical trial database; provides support to Medical Reviewer(s) assigned to the trial
  • Reviews protocol deviations
  • Reviews RAE reports, writes and/or reviews SAE narratives, supports Pharmacovigilance team with outstanding safety queries, interacts with sponsor on site safety issues
  • Reviews IND/SUSAR Safety Reports, updates/amendments to essential trial records, and annual IND reports with sponsor data (per sponsor request)
  • Participates in management of trial-related committees (e.g., independent data monitoring committee (IDMC)/adjudication committees) as described in the corresponding trial-specific charter(s)
  • Supports Pharmacovigilance, Medical Data Review and Data Management with reconciliation of safety and operational clinical trial databases
  • Reviews clinical study reports (CSRs), including safety narratives and tables, figures, and listings (TFLs)
  • Provides medical expertise on an as-needed basis in trials where medical monitoring is not a contract deliverable
  • Prepares for and participates in trial audits, follows up on audit findings
  • Participates in feasibility assessment of potential and ongoing trials in the country/region
  • Participates in bid defense meetings and other interactions with clients
  • Acts as a medical expert and provides therapeutic expertise to other PSI departments
Qualifications
  • Medical Doctor degree required
  • US Board Certification in Gastroenterology required
  • Experience as a practicing Gastroenterology (minimum of 10 years)
  • Clinical Research experience preferred
  • Proficiency with MS Office applications
  • Communication, presentation and analytical skills
  • Problem-solving, team and detail-oriented
Additional Information

As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.

Apply