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Medical Monitoring Jobs in California (NOW HIRING)

YO AI Labs

Clinicia Expert - Remote

Los Angeles, CA · 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

San Francisco, CA · 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

San Francisco, CA · 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

Palo Alto, CA · 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

San Jose, CA · 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 ...

Pfizer

Senior Medical Director, Hematology

La Jolla, CA · On-site

$274K - $457K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Conduct medical monitoring activities including eligibility assessment, datareviewand safety monitoring. * Lead peer-to-peer interactions withinvestigator. * Serve as the point of contact for ...

Lancesoft INC

Pharmacist

Whittier, CA · On-site

$3.2K - $3.3K/wk

Inpatient & clinical dosing (anticoagulants, cardiac, renal, geriatrics, pediatrics) Warfarin dosing, therapeutic med monitoring Pain control, psychotherapeutic management Compounding, IV piggybacks ...

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All JobsMedical Monitoring JobsMedical Monitoring Jobs in California

Medical Monitoring information

See California salary details

$20.7K

$91.3K

$175.7K

How much do medical monitoring jobs pay per year?

As of Aug 15, 2026, the average yearly pay for medical monitoring in California is $91,343.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,400.00 and $83,400.00 per year, depending on experience, location, and employer.

What is medical monitoring?

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 medical monitoring, 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 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.

What are the most commonly searched types of Medical Monitoring jobs in California?

The most popular types of Medical Monitoring jobs in California are:

What are popular job titles related to Medical Monitoring jobs in California?

For Medical Monitoring jobs in California, the most frequently searched job titles are:

What job categories do people searching Medical Monitoring jobs in California look for?

The top searched job categories for Medical Monitoring jobs in California are:

Medical Monitoring jobs near you
Infographic showing various Medical Monitoring job openings in California as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, 2% Temporary, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $91,343 per year, or $43.9 per hour.

Clinicia Expert - Remote

YO AI Labs

Los Angeles, CA • Remote

$150 - $200/hr

Full-time

Posted 4 days ago

Job description

Job Title: Clinician 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.