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Part Time Remote Clinical Trials Jobs in Raleigh, NC

micro1 AI

Biostatistician

Raleigh, NC · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor ...

IQVIA

Clinical Trial Rater

Raleigh, NC · Remote

Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Trial Rater

Durham, NC · Remote

Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

Talkiatry

Psychiatrist - Part Time/Full Time

Cary, NC · Remote

$325K - $375K/yr

This job is full time or part time Talkiatry is a clinician-led, virtual psychiatry practice built ... Minimal administrative burden in a fully remote, outpatient model What your day-to-day practice ...

Talkiatry

Psychiatrist - Part Time/Full Time

Raleigh, NC · Remote

$325K - $375K/yr

This job is full time or part time Talkiatry is a clinician-led, virtual psychiatry practice built ... Minimal administrative burden in a fully remote, outpatient model What your day-to-day practice ...

Talkiatry

Psychiatrist - Part Time/Full Time

Durham, NC · Remote

$325K - $375K/yr

This job is full time or part time Talkiatry is a clinician-led, virtual psychiatry practice built ... Minimal administrative burden in a fully remote, outpatient model What your day-to-day practice ...

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All JobsClinical Trials JobsPart Time Remote Clinical Trials JobsPart Time Remote Clinical Trials Jobs in Raleigh, NC

Part Time Remote Clinical Trials information

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How much do part time remote clinical trials jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for part time remote clinical trials in Raleigh, NC is $60.77, according to ZipRecruiter salary data. Most workers in this role earn between $49.33 and $68.46 per hour, depending on experience, location, and employer.

What is a part time remote clinical trials job?

Part-time remote clinical trials jobs involve supporting or managing clinical research studies from a remote location, often requiring fewer hours than full-time positions. These roles can include data entry, patient recruitment, regulatory documentation, study coordination, and monitoring, all performed online or by phone. They are ideal for those seeking flexible work arrangements, such as students, caregivers, or professionals with other commitments. Employers typically look for candidates with experience in clinical research, strong organizational skills, and proficiency with digital tools used in trial management.

What are the key skills and qualifications needed to thrive as a part time remote clinical trials coordinator, and why are they important?

A solid background in life sciences or healthcare, experience in clinical research, and familiarity with Good Clinical Practice (GCP) guidelines are essential for a part-time remote clinical trials role. Proficiency with electronic data capture (EDC) systems, remote monitoring tools, and regulatory documentation platforms is typically required. Excellent organizational skills, attention to detail, and strong communication are crucial for managing trial protocols and collaborating with dispersed teams. These skills ensure compliance, data integrity, and effective trial management in a remote and flexible work environment.

What are some common challenges faced by part time remote professionals in clinical trials, and how can they be addressed?

Part-time remote professionals in clinical trials often encounter challenges such as coordinating effectively with on-site teams, managing time zone differences, and maintaining clear communication for protocol updates or data queries. To address these challenges, it’s important to establish regular virtual check-ins, utilize collaborative project management tools, and stay proactive about communication. Being organized and responsive helps ensure that trial milestones are met and that remote contributions remain integral to the study’s success.

What are the most commonly searched types of Remote Clinical Trials jobs in Raleigh, NC?

The most popular types of Remote Clinical Trials jobs in Raleigh, NC are:

What are popular job titles related to Part Time Remote Clinical Trials jobs in Raleigh, NC?

For Part Time Remote Clinical Trials jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Part Time Remote Clinical Trials jobs in Raleigh, NC look for?

The top searched job categories for Part Time Remote Clinical Trials jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Part Time Remote Clinical Trials jobs?

Cities near Raleigh, NC with the most Part Time Remote Clinical Trials job openings:

Part Time Remote Clinical Trials jobs near you
Infographic showing various Part Time Remote Clinical Trials job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 13% Part Time, and 7% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $126,404 per year, or $60.8 per hour.

Biostatistician

Raleigh, NC • Remote

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

$60 - $65/hr

Part-time

Re-posted 12 days ago

Job description

Role Title: Biostatistician


Role Type: Contractor


Location: Remote


micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. 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 deriving, reproducing, or validating statistical outputs from clinical datasets and associated tables, figures, and listings (TFLs).
  2. Apply expert judgment to assess the correctness and consistency of reported estimates, confidence intervals, p-values, analysis populations, and missing data handling in alignment with the statistical analysis plan (SAP).
  3. Identify discrepancies between statistical outputs and their narrative descriptions in clinical study reports (CSR), including subtle errors in population definitions, censoring rules, or multiplicity handling.
  4. Establish defensible ground truth for each evaluation task, documenting the derivation process to enable independent verification.
  5. Provide structured written rationales distinguishing true statistical errors from acceptable methodological alternatives, employing clear and concise communication.
  6. Collaborate with a multidisciplinary project team, providing statistical insights and feedback as needed to refine evaluation tasks and criteria.


Preferred Qualifications

  1. 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit.
  2. Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets.
  3. Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies under ICH E9(R1).
  4. Proficiency in SAS and/or R, with the ability to independently reproduce analyses from written specifications.
  5. Ability to interpret SAPs and ensure reported results are consistent with pre-specified analyses.
  6. Advanced degree (MSc or PhD) in Biostatistics, Statistics, or a closely related quantitative field.
  7. Nice to have: Experience as lead statistician on pivotal/registrational studies, authoring or reviewing CSR statistical sections, oncology endpoint expertise, and exposure to AI-assisted statistical review tools.

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