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Remote Clinical Trial Transparency 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 ...

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 ...

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 ...

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 ...

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Remote Clinical Trial Transparency information

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

As of Aug 14, 2026, the average hourly pay for remote clinical trial transparency 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 some common challenges faced by professionals in a remote clinical trial transparency role, and how can they be addressed?

Professionals in Remote Clinical Trial Transparency roles often encounter challenges such as managing large volumes of sensitive data, ensuring regulatory compliance across multiple jurisdictions, and coordinating with global stakeholders virtually. Effective organization, strong communication skills, and staying up to date with evolving regulations are key to addressing these challenges. Utilizing secure data management platforms and fostering clear communication channels with cross-functional teams can help ensure both transparency and compliance in a remote environment.

What are the key skills and qualifications needed to thrive as a remote clinical trial transparency specialist?

To thrive as a Remote Clinical Trial Transparency Specialist, you need a solid understanding of clinical research processes, regulatory requirements (like FDA, EMA, or ICMJE), and often a degree in life sciences or healthcare. Familiarity with trial disclosure platforms (such as ClinicalTrials.gov and EudraCT), document management systems, and data anonymization tools is typically required. Strong attention to detail, analytical thinking, and effective written communication are crucial soft skills for ensuring accuracy and compliance. These abilities are vital to uphold regulatory standards, protect patient privacy, and promote trust through transparent clinical trial reporting.

What is a remote clinical trial transparency professional?

A Remote Clinical Trial Transparency professional is responsible for ensuring that information about clinical trials is accurately disclosed and made accessible to the public, regulators, and other stakeholders while working remotely. Their work involves preparing, reviewing, and submitting clinical trial data, maintaining compliance with global regulations, and protecting patient confidentiality. They ensure transparency by posting trial results to public registries, responding to disclosure requests, and supporting ethical standards in clinical research.

What is the difference between Remote Clinical Trial Transparency vs Remote Clinical Data Manager?

AspectRemote Clinical Trial TransparencyRemote Clinical Data Manager
Primary FocusEnsuring transparency of clinical trial results and compliance with reporting regulationsManaging and cleaning clinical trial data for analysis and reporting
Required CredentialsRegulatory knowledge, clinical trial experience, often a degree in life sciencesBiostatistics, data management certifications, degree in health sciences or related field
Work EnvironmentRemote, regulatory agencies, pharmaceutical companies, CROsRemote, pharmaceutical companies, CROs, data management teams

While both roles operate remotely within the clinical research industry, Remote Clinical Trial Transparency focuses on reporting compliance and transparency of trial results, whereas Remote Clinical Data Managers handle the technical aspects of data collection and management. Both require knowledge of clinical processes but serve different functions in the clinical trial lifecycle.

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The most popular types of Clinical Trial Transparency jobs are:

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The top searched job categories for Remote Clinical Trial Transparency jobs are:

Remote Clinical Trial Transparency jobs near you
Infographic showing various Remote Clinical Trial Transparency job openings in the United States as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. 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

Full-time

Re-posted 15 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