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Remote Clinical Trial Auditor Jobs (NOW HIRING)

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... Support the operational strategy related to assigned vendors, data flow, drug supply, remote ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research ...

CareDx, Inc.

Clinical Trial Manager

Brisbane, CA · Remote

Minimum of 4 years of clinical trial management and 2+ years clinical research associate with on-site/remote clinical monitoring experience in the biotechnology/pharmaceutical/CRO industry. * Minimum ...

Allucent

Clinical Trial Lead

Cary, NC · Remote

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

SummaryThe 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 ...

CTI

Clinical Trial Manager

Covington, KY · Remote

Oversee the core clinical portions of the Trial Master File and ensure they are up-to-date and ... May conduct on-site or remote monitoring activities as needed, including, but not limited to, Pre ...

CTI

Clinical Trial Manager

Covington, KY · On-site +1

Oversee the core clinical portions of the Trial Master File and ensure they are up-to-date and ... May conduct on-site or remote monitoring activities as needed, including, but not limited to, Pre ...

Braveheart Bio

Clinical Trial Manager

San Francisco, CA · On-site +1

$140K - $170K/yr

The Clinical Trial Manager (CTM) is a key member of the Clinical Operations team and will report ... This position is for remote work and may require domestic or international travel up to 25% (as ...

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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:
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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 Manager

Kardigan

Princeton, NJ • Remote

Full-time

Re-posted 9 days ago

Job description

Kardigan is seeking a Clinical Trial Manager to contribute to the planning, oversight and delivery of its cardiovascular clinical studies. As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to the asset's Clinical Trial or Clinical Program Lead. This position will be responsible for the oversight and management of Clinical Research Organizations (CROs) and vendors and will work cross-functionally on the trial operations' strategy and related initiatives. This role is pivotal in ensuring key project deliverables, primarily from CROs and vendors, are met according to the budget, timelines and quality standards (as defined by regulations, SOPs, and ICH-GCP) with the overall goal of developing new and innovative treatments for cardiovascular diseases with unmet need.

 4 Day Onsite Schedule - M - Th

Responsibilities

  • Supports the Clinical Trial Lead (CTL) in the oversight and management of study CROs to ensure that the study(ies) are completed on time, within budget, and in compliance with SOPs, FDA regulations and ICH/GCP guidelines
  • Coordinates and contributes to the review of relevant study plans and documents including protocols, informed consent forms, project management and monitoring plans, vendor study documents
  • Responsible for management of select study vendors including review of vendor study operational plans, key performance metrics, risks identification and mitigation
  • Proactively escalates issues to the Clinical Trial Lead to ensure timely resolution of issues and overall inspection readiness
  • Develops and coordinates the review and maintenance of vendor oversight plans in conjunction with the Clinical Trial Lead and other trial team members
  • Supports the Clinical Trial Lead in planning and maintaining study timelines, ensuring the cross functional project team remains on track for project and study deliverables
  • Actively participate in CRO and vendor meetings and study execution meetings
  • Support the operational strategy related to assigned vendors, data flow, drug supply, remote patient monitoring and any/all decentralized trial processes
  • Tracks, monitors and reports on study progress
  • Manages CRO and vendor budgets and invoicing procedures according to study contract
  • Summarizes CRO and vendor performance data and escalates risk to the Clinical Operations Program Lead and/or Head of Development Operations, as needed
  • Responsible for maintaining Action/Decision and Issue/Issue Resolution logs for assigned CRO/vendor management
  • Ensure CAPAs are in place, if applicable
  • Contribute to inspection readiness activities that support audits and regulatory inspections related to clinical trial conduct

Here's what you'll bring to the table

  • BA/BS with  7+ years of experience in global clinical trial management roles from pharmaceutical companies and/or CROs
  • Experience within the field of cardiovascular studies and/or rare disease is desirable
  • Experience in early and late stage drug development; late-stage development is desirable
  • Independent professional who proactively communicates frequently and effectively
  • Detail and action-oriented, organized and committed to quality and consistency
  • Ability to work successfully in cross-functional teams
  • Ability to work in a dynamic environment with a high degree of flexibility
  • Expertise in Microsoft Smartsheets desired
  • Experience in ICH/GCP inspections, audits and inspection preparedness
  • 20% of travel required

Apply