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Remote Clinical Trial Internship Jobs (NOW HIRING)

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 ...

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 ...

Clinical Trial Manager

San Francisco, CA ยท 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 ...

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 ...

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 ...

Clinical Trial Management Associate

Carlsbad, CA ยท On-site +1

$34.50 - $47.25/hr

We continue to invest time, money and energy into making our onsite, hybrid and remote work ... The Clinical Trial Management Associate (CTMA) works as part of the Study Management Team to ...

Clinical Trial Manager

San Francisco, CA ยท 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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Remote Clinical Trial Internship information

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

As of Jul 26, 2026, the average hourly pay for remote clinical trial internship in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

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

AspectRemote Clinical Trial InternshipRemote Clinical Research Coordinator
Required CredentialsTypically students or recent graduates; some may have relevant courseworkUsually requires a degree in health sciences or related field; certification may be preferred
Work EnvironmentRemote, often part-time or temporary; supervised by professionalsRemote or hybrid; involves coordinating trial activities and communication with sites
Employer & Industry UsagePharmaceutical companies, CROs, research institutions; entry-level rolePharmaceutical companies, CROs, hospitals; more operational responsibilities

While both roles involve clinical research, a Remote Clinical Trial Internship is typically an entry-level, temporary position for students or recent graduates gaining exposure. In contrast, a Remote Clinical Research Coordinator has more responsibilities, often requiring relevant education and certification, focusing on managing trial activities remotely or on-site.

More about Remote Clinical Trial Internship jobs
What cities are hiring for Remote Clinical Trial Internship jobs? Cities with the most Remote Clinical Trial Internship job openings:
What are the most commonly searched types of Remote Clinical Trial jobs? The most popular types of Remote Clinical Trial jobs are:
What states have the most Remote Clinical Trial Internship jobs? States with the most job openings for Remote Clinical Trial Internship jobs include:
Infographic showing various Remote Clinical Trial Internship job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Clinical Trial Manager

Kardigan

Princeton, NJ โ€ข Remote

Other

Posted 25 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.

ย 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 withย  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