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Hourly Remote Clinical Informatics Jobs in Miami, FL

Clinicia Expert - Remote

Miami, FL · Remote

$150 - $200/hr

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 ...

ABOUT THE ROLE The Clinical Application Support Analyst is an experienced healthcare professional ... Primarily remote work with occasional in-office work (Florida area residents only) * Travel ...

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Hourly Remote Clinical Informatics information

See Miami, FL salary details

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$47

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How much do hourly remote clinical informatics jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for hourly remote clinical informatics in Miami, FL is $47.11, according to ZipRecruiter salary data. Most workers in this role earn between $37.93 and $59.57 per hour, depending on experience, location, and employer.

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The most popular types of Remote Clinical Informatics jobs in Miami, FL are:

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For Hourly Remote Clinical Informatics jobs in Miami, FL, the most frequently searched job titles are:

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What cities near Miami, FL are hiring for Hourly Remote Clinical Informatics jobs?

Cities near Miami, FL with the most Hourly Remote Clinical Informatics job openings:

Infographic showing various Hourly Remote Clinical Informatics job openings in Miami, FL as of August 2026, with employment types broken down into 4% As Needed, 80% Full Time, 12% Part Time, and 4% Contract. Highlights an 72% In-person, 4% Hybrid, and 24% Remote job distribution, with an average salary of $97,996 per year, or $47.1 per hour.

Clinicia Expert - Remote

YO AI Labs

Miami, FL • Remote

$150 - $200/hr

Full-time

Posted 26 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.