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Medical Monitor Consultant Jobs (NOW HIRING)

Catholic Health

Monitor Technician

West Islip, NY · On-site

$26.82 - $34.86/hr

... with consultation of nursing &/or physician. * Appropriately documents and updates patient ... Assisting with the training of new staff in medical monitoring systems. * Technician will assist ...

Catholic Health

Monitor Technician

West Islip, NY

$26.82 - $34.86/hr

... with consultation of nursing &/or physician. * Appropriately documents and updates patient ... Assisting with the training of new staff in medical monitoring systems. * Technician will assist ...

Catholic Health

Monitor Tech

Roslyn, NY · On-site

$25.23/hr

... with consultation of nursing &/or physician. * Appropriately documents and updates patient ... Assisting with the training of new staff in medical monitoring systems. * Technical will assist ...

Catholic Health

Monitor Technician

West Islip, NY · On-site

$26.82 - $34.86/hr

... with consultation of nursing &/or physician. * Appropriately documents and updates patient ... Assisting with the training of new staff in medical monitoring systems. * Technician will assist ...

Catholic Health

Monitor Tech

Roslyn, NY · On-site

$25.23/hr

... with consultation of nursing &/or physician. * Appropriately documents and updates patient ... Assisting with the training of new staff in medical monitoring systems. * Technical will assist ...

InteleHealth

Medical Consultant

... medical advice. Maintain professional standards throughout every consultation. * Clinical ... Monitor patients requiring continued care or referral. Escalate cases where the patient's condition ...

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Medical Monitor Consultant information

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$31K

$148.2K

$399K

How much do medical monitor consultant jobs pay per year?

As of Sep 14, 2026, the average yearly pay for medical monitor consultant in the United States is $148,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $97,500.00 and $181,500.00 per year, depending on experience, location, and employer.

What is a medical monitor consultant?

Medical Monitor Consultants are licensed physicians who provide oversight and expert guidance during clinical trials to ensure participant safety and data integrity. They review adverse events, assess protocol compliance, and often serve as the primary point of contact for medical questions from study teams. Their expertise helps ensure that the study meets regulatory standards and that any risks to patient safety are managed appropriately. Medical Monitor Consultants play a critical role in maintaining ethical and scientific rigor throughout the clinical research process.

What are the key skills and qualifications needed to thrive as a medical monitor consultant?

To excel as a Medical Monitor Consultant, you typically need a medical degree (MD, DO, or equivalent), clinical experience, and in-depth knowledge of clinical trial protocols and regulatory requirements. Familiarity with clinical data management systems, safety databases, and Good Clinical Practice (GCP) guidelines is crucial. Strong analytical thinking, attention to detail, and effective communication skills help ensure clear reporting and interpretation of clinical data. These competencies are vital for safeguarding patient safety, ensuring compliance, and maintaining data integrity throughout clinical trials.

What are the typical challenges faced by a medical monitor consultant when overseeing clinical trials?

Medical Monitor Consultants often encounter challenges such as managing complex safety data, addressing unexpected adverse events, and ensuring timely communication between study teams, sponsors, and regulatory bodies. They must balance maintaining patient safety with the need to keep trials on track, which can require quick, evidence-based decision-making under pressure. Additionally, adapting to diverse therapeutic areas and varying sponsor protocols can make the role demanding but also rewarding for professionals seeking variety and impact in their work.

What cities are hiring for Medical Monitor Consultant jobs?

Cities with the most Medical Monitor Consultant job openings:

What states have the most Medical Monitor Consultant jobs?

States with the most job openings for Medical Monitor Consultant jobs include:

What are popular job titles related to Medical Monitor Consultant jobs?

For Medical Monitor Consultant jobs, the most frequently searched job titles are:

Infographic showing various Medical Monitor Consultant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $148,159 per year, or $71.2 per hour.

Senior Medical Consultant

San Diego, CA

Kumquat Biosciences Inc
Biotechnology Research and Development • 11 - 50 employees
Learn more about Kumquat Biosciences Incexternal

Full-time

Posted 23 days ago

Job description

Description

The Senior Medical Consultant (SMC) will work as a strategic partner with members of the senior executive team to develop and advance their clinical development strategy and drive the clinical research vision and regulatory roadmap for the company.


The SMC will direct the development of clinical strategies and programs, formulating standards and policies to maximize the potential for success of compounds under development. Primary responsibilities will include developing a target product profile and development plan, executing clinical trials, coordinating with clinical research organizations and other vendors, developing and managing clinical advisory boards, broadening the internal clinical research capabilities, and overseeing all clinical collaboration efforts with partners, principal investigators, and key opinion leaders. Our ideal candidate will have small molecule drug development experience in the fields of Immunology and Inflammation. 

Requirements

  • Provide insight and guidance with respect to all clinical and medical needs for the strategic direction and new business opportunities across the varied segments of interest for the Company.  
  • Provide oversight and leadership of the various functional areas within clinical operations, clinical science, medical monitoring, and regulatory affairs consistent with development goals across the company's portfolio. 
  • Drive execution of clinical trial plans to deliver compelling safety, pharmacokinetic, and efficacy data supportive of regulatory and marketing proof-of-relevance. 
  • Establish and maintain relationships with principal investigators, consultants and KOLs to ensure that the Company has a clear understanding of clinician needs and requirements, as well as medical practice patterns. 
  • Maintain an understanding of competitors and clinical developments in relevant therapeutic areas by attending scientific meetings and tracking literature. 
  • Actively assist in seeking product and/or technology alliances with appropriate pharmaceutical company partners to enhance/expedite the development of the company's assets. 
  • Help to establish and maintain collaborations with partners in academia, government, and industry. 

Apply