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Part Time Medical Monitor Clinical Trial Jobs in Appleton, WI

micro1 AI

Director of Biostatistics

Green Bay, WI · Remote

$60 - $100/hr

... clinical trial analysis, regulatory submission reviews, and observational study assessments ... academic medical contexts. * Demonstrated command of clinical study design, regulatory ...

micro1 AI

Biostatistician

Green Bay, WI · Remote

$60 - $100/hr

... clinical trial analysis, regulatory submission reviews, and observational study assessments ... academic medical contexts. * Demonstrated command of clinical study design, regulatory ...

State of Wisconsin

Nurse Clinician 3 - Part Time

Oshkosh, WI · On-site +1

$47.04 - $57.23/hr

The Department of Corrections is currently recruiting to fill multiple Part Time Nurse Clinician 3 ... medical services, developing and monitoring of treatment plans, coordinating treatment plans with ...

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Part Time Medical Monitor Clinical Trial information

See Appleton, WI salary details

$11

$36

$67

How much do part time medical monitor clinical trial jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for part time medical monitor clinical trial in Appleton, WI is $36.75, according to ZipRecruiter salary data. Most workers in this role earn between $25.10 and $46.92 per hour, depending on experience, location, and employer.

What is a part time medical monitor in a clinical trial?

A part time medical monitor in a clinical trial is a licensed physician who oversees the safety of participants and the integrity of clinical data, but does so without committing to a full-time schedule. They review adverse event reports, ensure the trial follows ethical guidelines, and provide medical expertise on patient safety issues as needed. Their flexible role allows them to support multiple studies or balance other professional responsibilities while still playing a critical part in clinical research.

What are the key skills and qualifications needed to thrive as a part time medical monitor in a clinical trial?

To thrive as a Part Time Medical Monitor in a clinical trial, you need a medical degree (MD or equivalent), expertise in clinical research, and a strong understanding of Good Clinical Practice (GCP) guidelines. Familiarity with electronic data capture (EDC) systems, safety reporting platforms, and relevant certifications such as GCP training are typically required. Excellent attention to detail, critical thinking, and effective communication skills help you navigate complex safety issues and collaborate with multidisciplinary teams. These competencies are essential for ensuring patient safety, regulatory compliance, and the overall integrity of clinical trials.

What are some common challenges faced by part-time medical monitors in clinical trials?

Part-time Medical Monitors in clinical trials often face challenges related to balancing multiple responsibilities across different studies or employers. They must stay up-to-date with protocol changes, quickly review and respond to safety data, and ensure timely communication with study teams despite limited hours. Effective time management and clear communication are essential to coordinate with investigators, sponsors, and other stakeholders while maintaining compliance and participant safety. Adapting to varying team structures and trial phases can also require flexibility and strong organizational skills.

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For Part Time Medical Monitor Clinical Trial jobs in Appleton, WI, the most frequently searched job titles are:

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Cities near Appleton, WI with the most Part Time Medical Monitor Clinical Trial job openings:

Part Time Medical Monitor Clinical Trial jobs near you
Infographic showing various Part Time Medical Monitor Clinical Trial job openings in Appleton, WI as of August 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution, with an average salary of $76,445 per year, or $36.8 per hour.

Director of Biostatistics

Green Bay, WI • Remote

micro1 AI
Software Development • 11 - 50 employees
Learn more about micro1 AIexternal

$60 - $100/hr

Part-time

This job post has expired today. Applications are no longer accepted.

Job description

Role Title: Biostatistician


Role Type: Contractor


Location: Remote


micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI benchmarking. 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. Design and author expert-level evaluation tasks simulating real-world biostatistics challenges, such as clinical trial analysis, regulatory submission reviews, and observational study assessments.
  2. Source, construct, and curate authentic datasets including trial data, patient records, and protocol documents for task use.
  3. Define correct methodological solutions and defensible clinical interpretations for each evaluation scenario.
  4. Develop comprehensive, 35+ item rubrics to evaluate AI agent performance with respect to methodological rigor and clinical reasoning.
  5. Ensure all tasks reflect the complexity and depth of real-world biostatistics practice, avoiding simplified or textbook-style examples.
  6. Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific standards.


Preferred Qualifications

  1. MS or PhD in biostatistics, statistics, or epidemiology.
  2. 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts.
  3. Demonstrated command of clinical study design, regulatory documentation, and observational research methodologies.
  4. Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological datasets.
  5. Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.
  6. Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a plus.
  7. Excellent written communication skills and ability to author detailed grading rubrics and technical documentation.


Compensation Structure

Compensation is output-based; experts are paid per task that meets the project specifications. The time required to complete work may vary depending on the expert’s experience and workflow. Minimum submission requirements apply. Experts must submit a minimum of tasks per week.


Start Timeline & Availability

We typically fill roles within 48 hours and are looking for experts ready to jump in right away. If selected, we expect you to start your first tasks within 24–48 hours of completing onboarding.

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