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Medical Monitor Jobs in Chicago, IL (NOW HIRING)

YO AI Labs

Hematology Expert - Remote

Chicago, IL · Remote

$150 - $200/hr

Direct experience with clinical trials as an investigator, sub-investigator, medical monitor, safety physician, or clinical development physician. * Experience reviewing clinical trial documents ...

YO AI Labs

Oncology Expert - Remote

Chicago, IL · Remote

$150 - $200/hr

Direct experience with clinical trials as an investigator, sub-investigator, medical monitor, safety physician, or clinical development physician. * Experience reviewing clinical trial documents ...

YO AI Labs

Clinicia Expert - Remote

Chicago, IL · Remote

$150 - $200/hr

Direct experience with clinical trials as an investigator, sub-investigator, medical monitor, safety physician, or clinical development physician. * Experience reviewing clinical trial documents ...

YO AI Labs

Oncology Expert - Remote

Chicago, IL · Remote

$150 - $200/hr

Direct experience with clinical trials as an investigator, sub-investigator, medical monitor, safety physician, or clinical development physician. * Experience reviewing clinical trial documents ...

Insight

MONITOR TECHNICIAN

Chicago, IL · On-site

$19 - $21/hr

At Insight Hospital and Medical Center- Chicago, we believe there is a better way to provide ... Short Summary: The monitor technician works as a team member under the direction of the ...

Insight

MONITOR TECHNICIAN

Chicago, IL · On-site

$19 - $21/hr

At Insight Hospital and Medical Center- Chicago, we believe there is a better way to provide ... Short Summary: The monitor technician works as a team member under the direction of the ...

Troy School District 30-C

Bus Monitor

Plainfield, IL · On-site

$16.45/hr

Pre-employment medical examination, including drug/alcohol test and tuberculosis clearance * Pass a Regional Office of Education Fingerprint/Background Clearance including Federal Bureau of ...

CEDENT

Senior Clinical Project Manager

Chicago, IL · On-site

Drive daily vendor and site management, including collaboration with Study Medical Monitor and KOLs to determine the medical and scientific needs * Effectively communicate project-related information ...

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All JobsMedical Monitor JobsMedical Monitor Jobs in Chicago, IL

Medical Monitor information

See Chicago, IL salary details

$21.6K

$95.4K

$183.5K

How much do medical monitor jobs pay per year?

As of Sep 2, 2026, the average yearly pay for medical monitor in Chicago, IL is $95,421.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,100.00 and $87,100.00 per year, depending on experience, location, and employer.

What is a medical monitor?

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 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 are the most commonly searched types of Medical Monitor jobs in Chicago, IL?

The most popular types of Medical Monitor jobs in Chicago, IL are:

What are popular job titles related to Medical Monitor jobs in Chicago, IL?

For Medical Monitor jobs in Chicago, IL, the most frequently searched job titles are:

What job categories do people searching Medical Monitor jobs in Chicago, IL look for?

The top searched job categories for Medical Monitor jobs in Chicago, IL are:

What cities near Chicago, IL are hiring for Medical Monitor jobs?

Cities near Chicago, IL with the most Medical Monitor job openings:

Medical Monitor jobs near you
Infographic showing various Medical Monitor job openings in Chicago, IL as of August 2026, with employment types broken down into 82% Full Time, 12% Part Time, and 6% Contract. Highlights an 91% In-person, and 9% Remote job distribution, with an average salary of $95,421 per year, or $45.9 per hour.

Hematology Expert - Remote

YO AI Labs

Chicago, IL • Remote

$150 - $200/hr

Full-time

Posted 22 days ago

Job description

Job Title: Hematology Expert Remote

Job Type: Contractor
Location: Remote

Job Overview

We are seeking experienced Clinicians specializing in Oncology and Hematology to contribute their medical expertise to an innovative healthcare AI project. In this role, you will help improve next-generation AI systems by evaluating clinical content, reviewing trial data, and providing expert medical judgment. No prior AI experience is required—your clinical expertise and domain knowledge are what matter most.

Key Responsibilities

  • Author and review clinical evaluation tasks requiring advanced oncology and hematology expertise.

  • Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess medical accuracy.

  • Evaluate the clinical relevance of efficacy and safety conclusions, including endpoints and treatment outcomes.

  • Assess dose escalation strategies, dose-limiting toxicities, adverse event grading, attribution, and patient safety narratives.

  • Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible interpretations.

  • Provide structured, guideline-based written explanations of clinical reasoning and findings.

  • Support AI model training by delivering high-quality clinical evaluations and expert feedback.

Required Skills

  • Clinical Oncology

  • Clinical Hematology

  • Clinical Trial Evaluation

  • CTCAE Grading

  • RECIST

  • Lugano Criteria

  • IMWG Criteria

  • IWCLL Criteria

  • ELN Criteria

  • Outcome Endpoint Analysis (ORR, DoR, PFS, OS, MRD)

  • Dose Escalation Assessment

  • Adverse Event Grading & Attribution

Preferred Qualifications

  • Board certification or specialist registration in Medical Oncology and/or Hematology.

  • 5+ years of post-training clinical experience.

  • Direct experience with clinical trials as an investigator, sub-investigator, medical monitor, safety physician, or clinical development physician.

  • Experience reviewing clinical trial documents, including protocols, investigator brochures, clinical study reports, safety narratives, and DSMB/IDMC materials.

  • Strong understanding of oncology and hematology response criteria and clinical endpoints.

  • Excellent written communication skills with the ability to explain complex clinical concepts clearly.

  • Experience in medical monitoring, medical director roles, adjudication committees, or independent review committees is preferred.

  • Peer-reviewed publications or authorship of clinical trial manuscripts is a plus.

  • Experience with AI-assisted clinical review tools is an advantage.