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Hourly Remote Clinical Trial Manager 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 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 ...

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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 ...

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Senior Clinical Trial Manager (Oncology) - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Senior Clinical Trial Manager, Biotech - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

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Hourly Remote Clinical Trial Manager information

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How much do hourly remote clinical trial manager jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for hourly remote clinical trial manager 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 does an hourly remote clinical trial manager do?

An Hourly Remote Clinical Trial Manager oversees the planning, coordination, and execution of clinical trials for medical research, all while working remotely and being paid by the hour. Their responsibilities include ensuring that trials comply with regulatory guidelines, managing timelines and budgets, and communicating with research teams and sponsors. They use digital tools to monitor progress, address issues, and maintain high standards of data integrity. This role requires strong organizational skills, attention to detail, and the ability to collaborate effectively across virtual teams.

What are the key skills and qualifications needed to thrive as an hourly remote clinical trial manager, and why are they important?

To thrive as an Hourly Remote Clinical Trial Manager, you need expertise in clinical research processes, regulatory compliance, and project management, usually supported by a degree in life sciences and relevant clinical research certifications. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and tools such as Microsoft Project is essential. Strong communication, organizational skills, and self-motivation are crucial soft skills for coordinating dispersed teams and stakeholders remotely. These competencies ensure efficient trial execution, regulatory adherence, and seamless collaboration in a virtual environment.

What are some common challenges faced by hourly remote clinical trial managers, and how can they be addressed?

Hourly Remote Clinical Trial Managers often face challenges related to communication and coordination across distributed teams, time zone differences, and maintaining oversight of trial progress without being on-site. To address these, leveraging robust digital project management tools, setting clear expectations for regular updates, and establishing strong lines of communication with site teams are crucial. Additionally, staying organized and proactive in addressing regulatory or documentation issues helps ensure that the trial stays on track and compliant with industry standards.

What is the difference between Hourly Remote Clinical Trial Manager vs Clinical Research Associate?

AspectHourly Remote Clinical Trial ManagerClinical Research Associate
CredentialsTypically requires a Bachelor's degree in life sciences, clinical research certification preferredUsually holds a Bachelor's degree in life sciences or related field, with some roles requiring certification
Work EnvironmentRemote, overseeing multiple sites and trial phasesPrimarily on-site or remote, monitoring clinical sites directly
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, medical device companies

The Hourly Remote Clinical Trial Manager focuses on overseeing entire trial processes remotely, managing teams and timelines, while the Clinical Research Associate primarily monitors clinical sites and ensures compliance. Both roles require similar educational backgrounds but differ in scope and daily responsibilities.

What cities are hiring for Hourly Remote Clinical Trial Manager jobs?

Cities with the most Hourly Remote Clinical Trial Manager job openings:

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

The most popular types of Remote Clinical Trial Manager jobs are:

What states have the most Hourly Remote Clinical Trial Manager jobs?

States with the most job openings for Hourly Remote Clinical Trial Manager jobs include:

Infographic showing various Hourly Remote Clinical Trial Manager 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 $130,034 per year, or $62.5 per hour.

Remote Clinical Trial Budget Manager

Sigma Systems, Inc.

Ridgefield, CT โ€ข Remote

Full-time

Posted 2 days ago

New


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