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Sub Investigator Remote Jobs (NOW HIRING)

YO AI Labs

Clinicia Expert - Remote

Los Angeles, CA · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Clinicia Expert - Remote

Boston, MA · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Clinicia Expert - Remote

Austin, TX · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Oncology Expert - Remote

San Francisco, CA · Remote

$150 - $200/hr

Oncology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Clinicia Expert - Remote

Boston, MA · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Clinicia Expert - Remote

San Francisco, CA · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Clinicia Expert - Remote

Washington, DC · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Clinicia Expert - Remote

San Jose, CA · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Clinicia Expert - Remote

Seattle, WA · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Hematology Expert - Remote

Dallas, TX · Remote

$150 - $200/hr

Hematology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Clinicia Expert - Remote

San Francisco, CA · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Oncology Expert - Remote

Austin, TX · Remote

$150 - $200/hr

Oncology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Clinicia Expert - Remote

Houston, TX · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Oncology Expert - Remote

Boston, MA · Remote

$150 - $200/hr

Oncology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Oncology Expert - Remote

Houston, TX · Remote

$150 - $200/hr

Oncology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Clinicia Expert - Remote

Philadelphia, PA · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Oncology Expert - Remote

Seattle, WA · Remote

$150 - $200/hr

Oncology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Clinicia Expert - Remote

Palo Alto, CA · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Clinicia Expert - Remote

Seattle, WA · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

YO AI Labs

Hematology Expert - Remote

San Jose, CA · Remote

$150 - $200/hr

Hematology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

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Sub Investigator Remote information

See salary details

$30.5K

$70.1K

$114K

How much do sub investigator remote jobs pay per year?

As of Aug 23, 2026, the average yearly pay for sub investigator remote in the United States is $70,123.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,000.00 and $85,000.00 per year, depending on experience, location, and employer.

What is a sub investigator in a remote clinical trial setting?

A Sub Investigator in a remote clinical trial is a medical professional who assists the Principal Investigator in conducting research studies, but works primarily from a remote location. They are responsible for ensuring protocol compliance, monitoring patient safety, collecting and reviewing data, and communicating with the study team. Remote Sub Investigators use digital tools and telemedicine platforms to oversee patient progress and maintain study integrity from a distance. This role is essential for decentralized trials, where patient visits and data collection occur outside traditional clinical sites.

How does a remote sub investigator effectively coordinate with on-site clinical trial teams?

A remote Sub Investigator typically collaborates with on-site clinical trial teams through regular virtual meetings, electronic data capture systems, and timely digital communication. Clear documentation, adherence to protocols, and proactive engagement are essential to ensure all study activities are conducted accurately and safely. Remote Sub Investigators often rely on strong organizational skills and the ability to foster trust with site coordinators and principal investigators to address challenges promptly. This collaborative approach helps maintain trial quality and regulatory compliance despite the physical distance.

What are the key skills and qualifications needed to thrive as a sub investigator remote, and why are they important?

To thrive as a Sub Investigator (Remote), you need a strong background in clinical research, medical or scientific education (often an MD, DO, or PhD), and experience with regulatory compliance and study protocols. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and remote monitoring tools is typically required. Strong attention to detail, effective communication, and organizational skills help ensure data integrity and collaboration with study teams. These skills are crucial for ensuring accurate study conduct, regulatory adherence, and successful remote trial management.

What is the difference between Sub Investigator Remote vs Clinical Research Associate?

AspectSub Investigator RemoteClinical Research Associate
CredentialsMedical degree or relevant healthcare backgroundHealthcare or life sciences degree, certification often preferred
Work EnvironmentRemote, often involved in patient data review and protocol oversightOn-site or remote monitoring at clinical trial sites
Industry UsageUsed in clinical trial oversight, especially in investigator-led studiesCommonly employed by CROs and pharmaceutical companies for site monitoring

While both roles are involved in clinical trials, a Sub Investigator Remote primarily supports trial oversight remotely, often with medical expertise, whereas a Clinical Research Associate typically conducts site monitoring and ensures compliance at trial sites. The roles overlap in industry and credentials but differ in work environment and specific responsibilities.

More about Sub Investigator Remote jobs

What cities are hiring for Sub Investigator Remote jobs?

Cities with the most Sub Investigator Remote job openings:

What are the most commonly searched types of Sub Investigator jobs?

The most popular types of Sub Investigator jobs are:

What states have the most Sub Investigator Remote jobs?

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Sub Investigator Remote jobs near you
Infographic showing various Sub Investigator Remote job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 86% Full Time, 9% Part Time, 2% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $70,123 per year, or $33.7 per hour.

Clinicia Expert - Remote

YO AI Labs

Los Angeles, CA • Remote

$150 - $200/hr

Full-time

Posted 11 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.