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Remote Clinical Trial Operations 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 ...

Legend Biotech USA, Inc.

$35.50 - $48.25/hr

Legend Biotech is seeking a Senior Clinical Trial Associate as part of the Clinical Operations team basedin Somerset, NJ.Location: RemoteRole OverviewWe are seeking a highly skilled and motivated ...

SAB

Clinical Sample Manager

Sioux Falls, SD · Remote

$130K - $150K/yr

Provide operational oversight of assigned clinical trial service providers, ensuring services are delivered according to study requirements, quality standards, and timelines. * Serve as the primary ...

Argenx

Trial Operations Excellence & Innovation Lead

... Clinical Trial Operations and ensuring organizational readiness in line with argenx vision. The ... Wearables and remote monitoring solutions; Hybrid and decentralized trial methodologies; AI-enabled ...

Vanguard Clinical

Clinical Operations Associate (Pool)

CA · Remote

$70K - $80K/yr

We are experts in clinical trial operations with a focus on Clinical Trial Management, CRO/Vendor Oversight, Trial Master File Management, Clinical Monitoring, Quality Assurance, Data Management and ...

Character Biosciences

Clinical Trial Manager

Development Operations Level: CTM - level 5 Location: Remote The Opportunity We're looking for an experienced, execution-focused Clinical Trial Manager to lead the day-to-day operational delivery of ...

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Remote Clinical Trial Operations information

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

As of Sep 3, 2026, the average hourly pay for remote clinical trial operations 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 the difference between Remote Clinical Trial Operations vs Remote Clinical Trial Coordinators?

AspectRemote Clinical Trial OperationsRemote Clinical Trial Coordinators
ResponsibilitiesOversees trial processes, manages site logistics, ensures complianceSupports trial activities, manages participant schedules, assists with data collection
Required CredentialsTypically requires a degree in life sciences, clinical research certificationOften requires a degree or certification in clinical research or related field
Work EnvironmentRemote, with collaboration across sites and teamsPrimarily remote, working closely with trial sites and participants
Industry UsageCommon in pharmaceutical and biotech companiesCommon in research organizations and CROs

Remote Clinical Trial Operations professionals focus on managing and overseeing the entire trial process, ensuring compliance and efficiency. In contrast, Remote Clinical Trial Coordinators handle day-to-day participant management and data collection. Both roles require clinical research knowledge and often work remotely, but their scope and responsibilities differ significantly.

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Remote Clinical Trial Operations jobs near you
Infographic showing various Remote Clinical Trial Operations job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, 13% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% 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 4 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