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Remote Clinical Trial Navigator 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 ...

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 ...

Ossium Health

Clinical Trial Manager

San Francisco, CA · On-site +1

$145K - $165K/yr

About the Job We are hiring a Clinical Trial Manager to support the successful execution of our ... as a remote work day * Ability to travel as needed (10% - 15%) * Qualified candidates must be ...

Fortrea

Clinical Trial Manager

Remote US or Canadian based. Job Overview: The Clinical Trial Manager has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project ...

Premier Research

$30 - $41/hr

Premier Research is looking for a Clinical Trial Associate to join our Clinical Monitoring, Site ... offered as remote based, however, there may be a need to come to the office occasionally for ...

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Ardelyx

Clinical Trial Manager

Waltham, MA · On-site +1

$136K - $160K/yr

The Clinical Trial Manager (CTM) is responsible for the end-to-end operational oversight of ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

$136K - $160K/yr

The Clinical Trial Manager (CTM) is responsible for the end-to-end operational oversight of ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

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 ...

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

As of Jul 30, 2026, the average hourly pay for remote clinical trial navigator in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Remote Clinical Trial Navigator, and why are they important?

To thrive as a Remote Clinical Trial Navigator, you need a solid understanding of clinical research protocols, patient recruitment, and healthcare regulations, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and compliance certifications such as Good Clinical Practice (GCP) are typically required. Exceptional communication, organizational skills, and empathy are vital for building trust with participants and coordinating across multidisciplinary teams. These skills are crucial for ensuring ethical conduct, smooth trial operations, and positive patient experiences in remote settings.

What are Remote Clinical Trial Navigators?

Remote Clinical Trial Navigators are professionals who guide patients, caregivers, or healthcare providers through the process of participating in clinical trials, all from a remote or virtual setting. They help identify suitable trials, assist with eligibility screening, explain trial protocols, and provide ongoing support throughout the trial process. By working remotely, they can serve a broader population, reduce barriers to clinical trial participation, and enhance patient engagement and retention. Their work is crucial in ensuring patients have access to potentially life-changing research treatments, regardless of their geographic location.

How does a Remote Clinical Trial Navigator typically collaborate with research teams and participants?

A Remote Clinical Trial Navigator plays a key role in facilitating communication between research teams and trial participants. They coordinate virtual meetings, provide guidance on trial protocols, and address participants' concerns, ensuring both compliance and a positive experience. Navigators often work closely with clinical coordinators, investigators, and data managers to track participant progress and resolve any logistical challenges. This collaborative approach helps streamline trial operations and supports participant retention.
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What cities are hiring for Remote Clinical Trial Navigator jobs? Cities with the most Remote Clinical Trial Navigator job openings:
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Remote Clinical Trial Navigator jobs near you
Infographic showing various Remote Clinical Trial Navigator job openings in the United States as of July 2026, with employment types broken down into 91% Full Time, 7% Part Time, and 2% Temporary. Highlights an 100% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Manager

Kardigan

Princeton, NJ • Remote

Other

Posted 29 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

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