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Remote Clinical Trial Auditor Jobs (NOW HIRING)

Allen Spolden

Clinical Trial Associate

Manhattan, NY · Remote

$55K - $65K/yr

This is a remote position. This role offers the opportunity to support the planning and execution ... Support the day-to-day coordination of clinical trials. * Maintain and organize Trial Master File ...

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Senior Clinical Trial Manager

Blue Bell, PA · Remote

Senior Clinical Trial Manager (Oncology) - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

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Senior Clinical Trial Manager

Blue Bell, PA · On-site +1

Senior Clinical Trial Manager, Biotech - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Fortrea

Remote US or Canadian based. We are seeking candidates with either CAR T or Ophthalmology experience. Job Overview: The Clinical Trial Manager has ownership in the clinical delivery and operational ...

CPC

Drug Supply/Clinical Trial Supply Manager

Aurora, CO · Remote

$70K - $90K/yr

We are looking for a Drug Supply/Clinical Trial Supply Manager to join our team! Responsible for ... Flexible and remote work schedules An Equal Opportunity Employer CPC provides equal employment ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

Summary The Senior Clinical Trial Manager will lead the day-to-day activities in a clinical trial ... Perform clinical research site activities, which can include onsite or remote monitoring, co ...

Vitalief

Clinical Trials Coverage Analyst

Chicago, IL · Remote

$70K - $85K/yr

... remote capacity, supporting a leading academic clinical research center in Chicago ... The ideal candidate brings strong expertise in Medicare billing guidelines, clinical trial ...

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Remote Clinical Trial Auditor information

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How much do remote clinical trial auditor jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for remote clinical trial auditor in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What is a remote clinical trial auditor?

A Remote Clinical Trial Auditor is a professional responsible for evaluating and ensuring compliance in clinical trials from a remote location. They review study documentation, processes, and data to verify adherence to regulatory requirements, Good Clinical Practice (GCP), and sponsor protocols. Their work helps maintain the integrity and reliability of clinical research, often using secure digital platforms to conduct audits without needing to visit trial sites in person. This role is vital for upholding ethical standards and ensuring patient safety during medical research.

How do remote clinical trial auditors typically collaborate with on-site teams during an audit?

Remote Clinical Trial Auditors often work closely with on-site clinical staff through virtual meetings, secure document sharing platforms, and regular email or phone communications. While they conduct most activities remotely, auditors rely on clear communication to review documentation, clarify procedures, and address compliance concerns. Successful auditors establish strong professional relationships with site coordinators to ensure efficient information exchange and to resolve any issues that arise during the audit process. This collaborative approach helps maintain audit quality and regulatory compliance, even without physical presence.

What is the difference between Remote Clinical Trial Auditor vs Remote Clinical Research Coordinator?

AspectRemote Clinical Trial AuditorRemote Clinical Research Coordinator
CertificationsGCP, RAC, or similarCRA certification, if applicable
Work EnvironmentReviewing trial sites remotely, auditing dataManaging trial activities, patient coordination
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, hospitals, clinical research organizations
Search & Comparison IntentUnderstanding auditing roles in clinical trialsManaging and coordinating clinical trial activities

The Remote Clinical Trial Auditor primarily focuses on reviewing trial data and ensuring compliance remotely, often auditing sites or data sources. In contrast, the Remote Clinical Research Coordinator manages trial logistics, patient interactions, and site activities. Both roles require knowledge of GCP and clinical trial processes but differ in daily responsibilities and focus areas.

What are the key skills and qualifications needed to thrive as a remote clinical trial auditor, and why are they important?

To thrive as a Remote Clinical Trial Auditor, you need in-depth knowledge of Good Clinical Practice (GCP), regulatory guidelines, clinical trial processes, and typically a background in life sciences or a related field. Familiarity with electronic trial master file (eTMF) systems, remote auditing tools, and relevant certifications such as CQA (Certified Quality Auditor) are often required. Excellent attention to detail, analytical thinking, and effective communication skills are crucial soft skills for this role. These competencies ensure accurate compliance assessments, facilitate clear reporting, and help maintain the integrity and quality of clinical research in a remote environment.
More about Remote Clinical Trial Auditor jobs
What cities are hiring for Remote Clinical Trial Auditor jobs? Cities with the most Remote Clinical Trial Auditor job openings:
What are the most commonly searched types of Clinical Trial Auditor jobs? The most popular types of Clinical Trial Auditor jobs are:
What states have the most Remote Clinical Trial Auditor jobs? States with the most job openings for Remote Clinical Trial Auditor jobs include:
What job categories do people searching Remote Clinical Trial Auditor jobs look for? The top searched job categories for Remote Clinical Trial Auditor jobs are:
Remote Clinical Trial Auditor jobs near you
Infographic showing various Remote Clinical Trial Auditor job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 100% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Clinical Trial Associate

Allen Spolden

Manhattan, NY • Remote

$55K - $65K/yr

Full-time

Posted 4 days ago

Job description

This is a remote position.

This role offers the opportunity to support the planning and execution of clinical trials while working collaboratively with cross-functional teams in the pharmaceutical, biotechnology, or contract research organization (CRO) industry.

Requirements

Candidates should possess an Associate's or Bachelor's degree in one of the following disciplines:

  • Psychology
  • Life Sciences
  • Biology
  • Biomedical Science
  • Public Health
  • Health Sciences
  • Nursing
  • Healthcare Administration
  • Medical Laboratory Science
  • Related scientific or healthcare disciplines


Requirements
  • Associate's or Bachelor's degree in a relevant field.
  • Clinical research experience preferred
  • Strong organizational and time management skills.
  • Excellent written and verbal communication skills.
  • High attention to detail.
  • Proficiency with Microsoft Office (Excel, Word, Outlook, and PowerPoint).
  • Ability to manage multiple priorities in a fast-paced environment.
  • Working knowledge of ICH-GCP guidelines and clinical research processes is preferred.
Key Responsibilities
  • Support the day-to-day coordination of clinical trials.
  • Maintain and organize Trial Master File (TMF) documentation.
  • Assist with regulatory document collection and tracking.
  • Coordinate communication with clinical sites, sponsors, and vendors.
  • Track study milestones, deliverables, and timelines.
  • Review study documentation for completeness and accuracy.
  • Support investigator meetings and study start-up activities.
  • Assist with data management and query resolution.
  • Ensure compliance with Good Clinical Practice (ICH-GCP), company SOPs, and regulatory requirements.
  • Prepare reports and maintain accurate study records.


BenefitsBenefits
  • Competitive hourly compensation
  • Flexible contract assignment
  • Opportunity to gain experience supporting clinical trials
  • Potential for contract extension based on business needs and performance