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Remote Medical Monitor Jobs in Renton, WA (NOW HIRING)

micro1 AI

Hematologist / Oncologist

Renton, WA · Remote

$160 - $200/hr

Remote micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer's project ... Previous roles in medical monitoring or as medical director on oncology or haematology programmes ...

New

micro1 AI

Clinician (Oncology / Hematology)

Federal Way, WA · Remote

$160 - $200/hr

Remote micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer's project ... Previous roles in medical monitoring or as medical director on oncology or haematology programmes ...

New

micro1 AI

Clinician (Oncology / Hematology)

Seattle, WA · Remote

$160 - $200/hr

Remote micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer's project ... Previous roles in medical monitoring or as medical director on oncology or haematology programmes ...

New

micro1 AI

Hematologist / Oncologist

Seattle, WA · Remote

$160 - $200/hr

Remote micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer's project ... Previous roles in medical monitoring or as medical director on oncology or haematology programmes ...

New

micro1 AI

Hematologist / Oncologist

Tacoma, WA · Remote

$160 - $200/hr

Remote micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer's project ... Previous roles in medical monitoring or as medical director on oncology or haematology programmes ...

New

micro1 AI

Clinician (Oncology / Hematology)

Tacoma, WA · Remote

$160 - $200/hr

Remote micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer's project ... Previous roles in medical monitoring or as medical director on oncology or haematology programmes ...

New

micro1 AI

Hematologist / Oncologist

Federal Way, WA · Remote

$160 - $200/hr

Remote micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer's project ... Previous roles in medical monitoring or as medical director on oncology or haematology programmes ...

New

micro1 AI

Hematologist / Oncologist

Bellevue, WA · Remote

$160 - $200/hr

Remote micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer's project ... Previous roles in medical monitoring or as medical director on oncology or haematology programmes ...

New

micro1 AI

Clinician (Oncology / Hematology)

Renton, WA · Remote

$160 - $200/hr

Remote micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer's project ... Previous roles in medical monitoring or as medical director on oncology or haematology programmes ...

New

micro1 AI

Clinician (Oncology / Hematology)

Kent, WA · Remote

$160 - $200/hr

Remote micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer's project ... Previous roles in medical monitoring or as medical director on oncology or haematology programmes ...

New

micro1 AI

Hematologist / Oncologist

Kent, WA · Remote

$160 - $200/hr

Remote micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer's project ... Previous roles in medical monitoring or as medical director on oncology or haematology programmes ...

New

micro1 AI

Clinician (Oncology / Hematology)

Bellevue, WA · Remote

$160 - $200/hr

Remote micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer's project ... Previous roles in medical monitoring or as medical director on oncology or haematology programmes ...

New

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All JobsMedical Monitor JobsRemote Medical Monitor JobsRemote Medical Monitor Jobs in Renton, WA

Remote Medical Monitor information

See Renton, WA salary details

$23.6K

$104.1K

$200.2K

How much do remote medical monitor jobs pay per year?

As of Aug 7, 2026, the average yearly pay for remote medical monitor in Renton, WA is $104,109.00, according to ZipRecruiter salary data. Most workers in this role earn between $95,000.00 and $95,000.00 per year, depending on experience, location, and employer.

How does a remote medical monitor effectively collaborate with clinical trial teams across different time zones?

As a Remote Medical Monitor, you will regularly coordinate with clinical research associates, investigators, and data management teams who may be located globally. Effective collaboration often involves flexible scheduling for virtual meetings, clear written communication, and proactive updates to ensure all team members are aligned. Utilizing project management tools and maintaining detailed documentation helps streamline workflows and reduce misunderstandings. Strong organizational skills are essential to manage time zone differences and ensure timely responses to safety queries or protocol deviations.

What is a remote medical monitor?

A Remote Medical Monitor is a healthcare professional, typically a physician, who oversees the safety and efficacy of clinical trials from a remote location. They are responsible for reviewing patient data, monitoring adverse events, and ensuring compliance with study protocols without being physically present at the trial site. Remote Medical Monitors play a crucial role in maintaining the integrity of clinical research, facilitating timely decisions, and ensuring patient safety. Their work allows for greater flexibility and efficiency in clinical trial management, especially in multi-site or decentralized studies.

What is the difference between Remote Medical Monitor vs Remote Clinical Research Associate?

AspectRemote Medical MonitorRemote Clinical Research Associate
Required CredentialsMedical degree or clinical background, certifications like CCRP or CCRA often preferredDegree in life sciences, healthcare, or related field; certifications like CCRP common
Work EnvironmentRemote, primarily reviewing clinical trial data and safety reportsRemote or onsite, overseeing trial sites and monitoring compliance
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, research institutions

While both roles support clinical trials remotely, Remote Medical Monitors focus on safety data review and medical oversight, whereas Remote Clinical Research Associates primarily oversee trial site activities and compliance. Both require healthcare or scientific backgrounds and are common in the pharmaceutical and biotech industries.

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

To thrive as a Remote Medical Monitor, you need a medical degree (MD or equivalent), clinical experience, and a strong understanding of clinical trial protocols and regulations. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification are typically required. Excellent analytical skills, attention to detail, and effective remote communication are vital soft skills for this role. These abilities ensure accurate oversight of patient safety and data integrity in decentralized clinical trials.
What are popular job titles related to Remote Medical Monitor jobs in Renton, WA? For Remote Medical Monitor jobs in Renton, WA, the most frequently searched job titles are:
What job categories do people searching Remote Medical Monitor jobs in Renton, WA look for? The top searched job categories for Remote Medical Monitor jobs in Renton, WA are:
What cities near Renton, WA are hiring for Remote Medical Monitor jobs? Cities near Renton, WA with the most Remote Medical Monitor job openings:
Remote Medical Monitor jobs near you

Hematologist / Oncologist

micro1 AI

Renton, WA • Remote

$160 - $200/hr

Part-time

Posted 3 days ago

New

Job description

Role Title: Clinician (Oncology / Hematology)


Role Type: Contractor


Location: Remote


micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer’s project at the forefront of AI in healthcare. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review evaluation tasks that require nuanced clinical judgment, leveraging Clinical Study Reports, periodic safety reports, and regulatory correspondence in oncology and haematology.
  2. Assess the clinical defensibility of efficacy and safety conclusions, ensuring endpoints and effect sizes reflect true clinical significance.
  3. Apply advanced judgment to dose escalation, dose-limiting toxicity, modifications, adverse event grading and attribution, and the coherence of patient narratives.
  4. Evaluate benefit-risk reasoning, scrutinizing the durability of conclusions in light of new events, and the realism of described management strategies.
  5. Identify and flag content that is clinically implausible or internally inconsistent, distinguishing these from legitimate clinical variation.
  6. Provide structured, guideline-based written rationales that clearly explain the validity or limitations of clinical interpretations for a non-clinical audience.


Preferred Qualifications

  1. Specialist registration or board certification in medical oncology and/or haematology, with 5+ years of post-training clinical experience.
  2. Direct involvement in clinical trials as investigator, sub-investigator, or sponsor-side medical monitor, safety physician, or clinical development physician.
  3. Proficiency with CTCAE grading, relevant response criteria (RECIST, Lugano, IMWG, IWCLL, ELN), and outcome endpoints (ORR, DoR, PFS, OS, MRD).
  4. Hands-on experience with trial documents such as protocols, investigator brochures, CSRs, safety narratives, or DSMB/IDMC materials.
  5. Demonstrated excellence in written communication, with clear, structured explanations of clinical reasoning tailored for non-clinical readers.
  6. Previous roles in medical monitoring or as medical director on oncology or haematology programmes, and committee participation (IDMC, DSMB, adjudication, or independent review committees).
  7. Peer-reviewed publication record or authorship on clinical trial manuscripts, with any exposure to AI-assisted clinical review tools seen as a plus.

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