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Medical Monitor Jobs (NOW HIRING)

IQVIA

Medical Director, Neurologist ( Part-Time)

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 ...

4D Molecular Therapeutics

Medical Director

$278K - $310K/yr

Serve as medical monitor for clinical studies, ensuring patient safety and data integrity. Author and review clinical documents including protocols, IBs, ICFs, INDs, CSRs, and regulatory submissions.

Invivyd

Medical Director

New Haven, CT · On-site

As the medical and scientific authority for one or more studies, you will be fully accountable for study design, execution, monitoring, delivery, and reporting, partnering closely with cross ...

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 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 · 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

$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 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 ...

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 ...

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Medical Monitor information

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How much do medical monitor jobs pay per year?

As of Jul 2, 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:
Who are the top companies hiring for Medical Monitor jobs? The top employers for 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 3% As Needed, 48% Full Time, 46% Part Time, and 3% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $92,555 per year, or $44.5 per hour.

Senior Medical Director

Bridge Bio Oncology Therapeutics

South San Francisco, CA • On-site

$266K - $319K/yr

Full-time

Posted 9 days ago

Job description

Description:
  • Serve as trial medical lead/medical monitor of assigned clinical studies, including contributing to site selection, study oversight and management plans, CRF design, ICF, enrollment, medical data review, CSR writing, and authoring of clinical modules and clinical review of other modules
  • Be a leader within and actively participate and contribute to the cross-functional and project teams meetings, including functioning as clinical representative
  • Cultivate relationships with clinical investigators, clinical consultants, and thought leaders for the execution of ongoing trials and developing opportunities
  • Serve as trial medical lead/medical monitor of assigned clinical studies, including contributing to site selection, study oversight and management plans, CRF design, ICF, enrollment, medical data review, CSR writing, and authoring of clinical modules and clinical review of other modules
  • Be a leader within and actively participate and contribute to the cross-functional and project teams meetings, including functioning as clinical representative
  • Cultivate relationships with clinical investigators, clinical consultants, and thought leaders for the execution of ongoing trials and developing opportunities
  • Help ensure Clinical Study Team compliance with ethical and GCP guidelines, and FDA, EMEA, ICH, and other regulatory requirements relevant to industry/country/region
  • Provide expert support for the preparation of clinical/study protocols and amendments, clinical trial documents
  • Responsible for the clinical sections of regulatory documents (investigator brochures, development safety update report, etc), clinical study reports
  • Conduct investigator meetings and lead site initiation visits with clinical trial investigators
  • Execute and deploy drug development strategic plans, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets
  • Translate findings from research and nonclinical studies into clinical development opportunities
  • Contribute to the clinical portions of writing and preparation of abstracts, presentations, and manuscripts
  • Attend key scientific congresses and meetings as requested in support of speakers and key opinion leaders
  • Remain current in relevant therapeutic areas and conversant with the literature as well as critical emerging data
  • Represent the Clinical Development team during interactions with regulatory agencies, as applicable
Requirements:
  • Trained MD and/or MD-Ph.D. degree
  • 7+ years of experience in drug development, either within the industry or as a clinical investigator/physician-scientist in academia, or equivalent experience; oncology experience is preferred
  • Patient-focused, with a deep commitment to understanding needs and improving the lives of patients, and a passion for developing novel therapeutics
  • Demonstrated ability to collaborate successfully with multiple functions in a team environment
  • Demonstrated record of accomplishment in a compressed time frame; capable of prioritizing tasks and delivering on deadlines with high-performance standards and attention to detail
  • Motivated to work in a fast-paced, high accountability, small company environment; a "can do" and collegial professional who leads through influence and interpersonal skills
  • Intellectually curious with the courage to challenge and seek new ways to improve work
  • Strong written and oral communication skills, including presentation skills
  • Ability to analyze and interpret data and develop written reports and presentations of those data
  • Solid critical, strategic, and analytical thinking skills
  • Experience in all aspects of study and protocol conduct, both early and late phase, including protocol writing, start-up, study execution, analysis, and reporting
  • Experience in working closely with investigative sites, including principal investigators, sub- investigators, study coordinators, and other site personnel involved in clinical trials

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