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Full Time Remote Clinical Trial 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 ...

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 ...

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 ...

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 ...

Clinical Trial Manager The Clinical Trial Manager (CTM) provides operational expertise and ... Flexible, inclusive culture - 70% remote workforce, 66% women-led teams * Learn more about our core ...

Clinical Trial Manager The Clinical Trial Manager (CTM) provides operational expertise and ... Flexible, inclusive culture - 70% remote workforce, 66% women-led teams * Learn more about our core ...

We are seeking a self-motivated Clinical Trial Manager to lead end-to-end delivery of clinical ... being remote or hybrid based out of our office in Wellesley, MA. Base salary offered may vary ...

Clinical Trial Associate

Redwood City, CA · On-site +1

$41 - $56/hr

The Clinical Trial Associate (CTA) supports CRAs, and study teams across Karius clinical studies by ... Remote (Bay Area preferred) Primary Responsibilities: * Assist study teams with the collection ...

Clinical Trial Associate

Redwood City, CA · On-site +1

$41 - $56/hr

The Clinical Trial Associate (CTA) supports CRAs, and study teams across Karius clinical studies by ... Remote (Bay Area preferred) Primary Responsibilities: * Assist study teams with the collection ...

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Full Time Remote Clinical Trial information

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$96

How much do full time remote clinical trial jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for full time remote clinical trial 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 is the difference between Full Time Remote Clinical Trial vs Full Time Remote Clinical Research Coordinator?

AspectFull Time Remote Clinical TrialFull Time Remote Clinical Research Coordinator
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRP are commonRequires similar degrees; often holds certifications like CCRP or CRC
Work EnvironmentConducted remotely, managing trial data, documentation, and communication with sitesPrimarily remote; coordinates trial activities, site management, and patient interactions
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch institutions, hospitals, CROs

While both roles involve clinical trial activities, the Full Time Remote Clinical Trial focuses on data management and trial oversight remotely, whereas the Clinical Research Coordinator handles site coordination and patient interactions, often requiring similar credentials and working in related environments.

What cities are hiring for Full Time Remote Clinical Trial jobs?

Cities with the most Full Time Remote Clinical Trial job openings:

What are the most commonly searched types of Remote Clinical Trial jobs?

The most popular types of Remote Clinical Trial jobs are:

Remote Clinical Trial Budget Manager

Sigma Systems, Inc.

Ridgefield, CT • Remote

Full-time

This job post has expired today. Applications are no longer accepted.


Job description

37561875 Remote Clinical Trial Budget Manager, Ridgefield, CT 12 Months
Sigma Systems is seeking a Remote Clinical Trial Budget Manager
Remote
Responsibilities:

  • The Clinical Trial Budget Manager is responsible for assurance that clinical trial /site budget is of high quality, and allocations are within fair market values.
  • This role is responsible for the development and maintenance of Sites Fee Framework as well as timely and accurate coordination, processing, monitoring, and administration of payments to sites according to budget and terms.
  • The incumbent will be responsible for the support of management goals and objectives of the department.
  • Ensures clinical trial site budget is of high quality and allocations are within fair market values (FMV); analyze protocol flowcharts to create costing, payment strategies, and budget estimates and negotiation prameters within FMV.
  • Drives development and maintenance of Site Fee Framework.
  • Sets up year-end accruals and developing plausibility checks.
  • Coordinates, processes, monitors and administers payments (invoice and visits) in accordance with agreed terms of Contracts and Budget Exhibits.
  • Sets up, closes, re-opens, and submits payments within all grants.
  • Effectively uses budget-specific and trial metrics and tools to report on, provide visibility into, and analyze performance and deliverables.
  • Maintains a focused continuous improvement culture by identifying and executing strategies and priorities to enable the Budget group to deliver value and enhance overall operational effectiveness.
  • Actively remains current with industry standards, trends, and competitive intelligence on budget best practices.
  • Interfaces across Medical, all TAs, Finance, Legal, and external parties e.g., investigators, site personnel, third party vendors.
  • Liaises within Clinical Trial Manager and TA Lead for review and approval of budget and payment decisions.
  • Supports Finance in reviewing any issues with payment execution based on agreed contract and ensuring matching of accrual statuses.
  • Liaises with Clinical Finance/Accounting Department, Legal Department (if needed) and the local Head of Clin Ops and/or Clinical Operations Management for approval of payment related decisions (e.g., standard payment frequency) and maintain proper documentation.
  • Partners with Contract Managers to identify issues and propose mitigations.
  • Supports contract manager in developing negotiation strategy for site budget.
  • Represents Budget group processes on local/global working groups.
  • Ensures commitment to customer-centric behaviors.
  • Maintains high degree of responsiveness to both internal and external requests.

Requirements:

  • Bachelor's degree with minimum of five (5) years of relevant business experience in regulated pharmaceuticals or healthcare industry.
  • Strong clinical background and budgeting understanding of cost drivers and benchmarks for clinical site budget.
  • Ability to think strategically and initiate strong and persuasive contractual arguments to support business policies and objectives.
  • Track record in setting priorities, organization and problem-solving skills which support and enable sound decision making.
  • Excellent customer service skills and high attention to detail.
  • Demonstrated analytical skills and critical thinking to resolve issues in a variety of complex situations requiring new solutions.
  • Excellent written and verbal communication skills and the ability to be clear and concise in a variety of communication settings.
  • Experience in working with systems, applications related to clinical and/or project management planning and reporting systems.
  • Excellent knowledge of computer applications (Excel, Word, Access) is essential.
  • Experience with Veeva and grant plan required