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Medical Monitoring Jobs (NOW HIRING)

Fortrea

$240K - $340K/yr

Responsible for supporting the development activities of proposed and ongoing projects in their area of expertise, as well as medical monitoring to assigned clinical studies. The (Senior) Medical ...

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 ...

IQVIA

Medical Director, Cardiology

Durham, NC · Remote

Medical Monitoring: * Primarily serves as Global and /or Regional Medical Advisor on assigned projects. * Serves as Scientific Advisor and provides guidance to Project Leaders on the medical and ...

Charlie Health

SUD Medical Director

New York, NY · Remote

Medical Monitoring & Clinical Oversight * Oversee the daily operations of the medical monitoring teams, ensuring real-time response to "red-flag" clinical data or physiological alerts. * Act as the ...

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$21K

$92.6K

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How much do medical monitoring jobs pay per year?

As of Jul 20, 2026, the average yearly pay for medical monitoring 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 a median annual salary of around $80,000 to $100,000, depending on experience, location, and the complexity of clinical trials. Salaries can range from approximately $60,000 for entry-level roles to over $120,000 for senior positions or those with specialized certifications. The role often requires knowledge of Good Clinical Practice (GCP) and regulatory guidelines.

What is the easiest medical job that pays well?

A medical monitoring role, such as a medical assistant or patient care technician, is generally considered easier to enter and offers decent pay compared to more specialized healthcare positions. These jobs often require a certification or short training program and involve tasks like patient intake, vital signs, and basic clinical support. While pay varies by location, these roles typically provide a good balance of accessibility and compensation in the healthcare field.

What is a Medical Monitoring job?

A Medical Monitoring job involves overseeing the safety and integrity of clinical trials by assessing adverse events, ensuring protocol compliance, and providing medical oversight. Professionals in this role, often physicians or healthcare experts, collaborate with clinical teams to evaluate patient safety data and regulatory reporting requirements. They play a crucial role in ensuring that trial participants are protected while maintaining the scientific validity of the study.

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

To thrive in Medical Monitoring, a strong background in clinical practice or life sciences, attention to detail, and critical thinking are essential, often supported by a relevant medical or scientific degree. Familiarity with safety databases, adverse event reporting systems, and tools for data analysis, as well as certifications such as GCP (Good Clinical Practice), are commonly required. Effective communication, decisiveness, and the ability to collaborate across multidisciplinary teams help individuals excel in this role. These skills ensure the accurate monitoring of clinical trials and patient safety, supporting compliance and the integrity of medical research.

What is a medically monitored position?

A medical monitoring position involves overseeing and ensuring the health and safety of individuals, often in healthcare, clinical, or research settings. It typically requires knowledge of medical protocols, certifications such as CPR or first aid, and the ability to respond quickly to medical emergencies.

What are the typical day-to-day responsibilities of someone working in Medical Monitoring?

In a Medical Monitoring role, your daily responsibilities often include reviewing data from ongoing clinical trials, assessing adverse event reports, providing medical expertise to study teams, and ensuring that patient safety is maintained throughout the research process. You may participate in meetings with investigators, contribute to protocol development, and respond to safety concerns as they arise. Collaboration with clinical research associates, data managers, regulatory personnel, and sponsors is common, requiring clear and timely communication. This role is integral to maintaining trial integrity, regulatory compliance, and ensuring participant well-being.

How to be a medical monitor?

A medical monitor is a healthcare professional responsible for overseeing clinical trial safety and compliance. To become one, typically a physician or licensed healthcare provider with experience in clinical research is required, along with knowledge of Good Clinical Practice (GCP) guidelines and relevant certifications. Strong communication skills and attention to detail are essential for monitoring patient safety and data integrity throughout a trial.
More about Medical Monitoring jobs
What cities are hiring for Medical Monitoring jobs? Cities with the most Medical Monitoring job openings:
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Medical Monitoring jobs near you
Infographic showing various Medical Monitoring job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $92,555 per year, or $44.5 per hour.
Sr. Medical Director, Rheumatology - US Remote

Sr. Medical Director, Rheumatology - US Remote

Fortrea

On-site, Remote

$240K - $340K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago

Fortrea rating

7.2

Company rating: 7.2 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

47th of 59 rated research

Job description

Senior Medical Director, Rheumatology - US Remote Based
Raising CRO standards for innovation and delivery to help bring life-changing treatments to patients faster. Fortrea is seeking a dedicated US remote based Medical Director or Senior Medical Director with deep expertise in Rheumatology along with background in innovative therapies, including cell and gene therapy. The incumbent will provide medical leadership and oversight across all phases of development, including early-phase innovation and late-phase global programs. Responsible for supporting the development activities of proposed and ongoing projects in their area of expertise, as well as medical monitoring to assigned clinical studies.
The (Senior) Medical Director will serve as a key medical representative in client interactions, business-development discussions, and proposal presentations. The role will further foster and enhance relationships with global clinical operations teams and provide leadership as the Leading Physician for Phase I-IV clinical trials).
We are particularly interested in candidates who have led or supported rheumatology clinical programs and who are comfortable serving as the study physician, providing medical monitoring oversight (e.g., safety review, contribution to protocol development, including study design, endpoints and eligibility criteria) and working collaboratively with other project team members. In addition to strong scientific leadership, the role is expected to be highly client-facing with an increased business development component - requiring regular engagement at executive level, and the confidence and polish to represent Fortrea with senior client leaders, external partners, and other key stakeholders.
WHAT YOU WILL DO
  • High level Medical TA and Clinical Trial Subject Matter Expertise (SME) contributions (may be Regional or Global).
  • SME Cross-functional, scientific & technical contributions and interactions with Clients Medical teams, Project teams, Key Opinion Leaders and at Principal Investigator/Site levels.
  • Partner with clients and internal teams to support business development - shaping clinical/medical strategy for proposals, bid defences, and client discussions.
  • Provide oversight of medical monitoring activities to ensure timelines and quality of medical deliverables and assigns physician resources as required.
  • According to the scope of work, may serve as Global Lead, Regional or Program Project Physician across multiple indications.
  • Provide subject matter and drug development expertise and is a key contributor to the medical strategy and execution of the study/program for the client.
  • Provides input, review and revision of protocols, case report forms, training materials, project specific tools, analysis plans design, clinical trial reports and new drug applications.
  • Prepares materials for and actively participates in investigator meetings and assists at site initiation visits.
  • Provides medical/scientific expertise to project team.
  • And any other duties as required or assigned.

YOU NEED TO BRING...
Qualifications (Minimum Required and preferred):
  • MD Degree
  • Board Certification in Internal Medicine
  • Specialization in Rheumatology and broader therapeutic experience in autoimmune diseases (AID)
  • Preferred: Specific expertise in cell and gene therapy in autoimmune diseases (AID)
  • 3+ years of substantial knowledge of drug development and extensive clinical research experience within the pharmaceutical/CRO industry (or as a clinical trial investigator)
  • Preferred: Industry experience inclusive of clinical trials medical monitoring experience or other relevant clinical development/trial experience at a CRO, pharmaceutical company, regulatory agency
  • Strong scientific communication and client-facing capabilities, including presenting scientific expertise, supporting proposals, and strengthening external partnerships
  • English language skills: Full professional proficiency

Work Environment
  • Remote position based in USA
  • Occasional national and international travel required, including attendance at sponsor meetings, investigator meetings, and relevant scientific or industry conferences.

Physical Requirements
  • Frequently stationary for 6-8 hours per day.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
  • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
  • Regular and consistent attendance.
  • Varied hours may be required.

Pay Range: USD $240,000-$340,000
Benefits: All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable.
Application Deadline: July 30, 2026
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Learn more about our EEO & Accommodations request here.

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