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Remote Clinical Trial Consulting Jobs (NOW HIRING)

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

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 ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

Clinical Trial Lead

Cary, NC ยท 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 ...

Clinical Trial Lead

Cary, NC ยท 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 ...

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 ...

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 ...

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Remote Clinical Trial Consulting information

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

As of Aug 23, 2026, the average hourly pay for remote clinical trial consulting 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 remote clinical trial consulting?

Remote clinical trial consulting involves providing expert guidance and support for clinical trials from a remote location, rather than on-site. Consultants in this field help pharmaceutical companies, research organizations, and healthcare providers design, manage, and monitor clinical trials. Their responsibilities may include protocol development, regulatory compliance, study management, data analysis, and ensuring ethical conduct. By working remotely, consultants can collaborate with global teams, leverage digital tools, and offer flexible, cost-effective solutions for clinical research projects.

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

To excel as a Remote Clinical Trial Consultant, you need expertise in clinical research protocols, regulatory compliance, and data analysis, typically supported by a degree in life sciences or a related field and experience in clinical trials. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like GCP (Good Clinical Practice) are highly valued. Strong communication, problem-solving, and organizational abilities are essential for collaborating with diverse teams and managing projects remotely. These skills and qualifications ensure trials run efficiently, adhere to regulatory standards, and produce reliable, high-quality results.

What are some common challenges faced by remote clinical trial consultants, and how can they be overcome?

Remote clinical trial consultants often encounter challenges such as coordinating across multiple time zones, maintaining clear communication with on-site teams, and ensuring data integrity when working virtually. To address these, consultants should leverage robust project management and communication tools, establish regular check-ins with stakeholders, and follow strict data security protocols. Building strong relationships with site staff and fostering a proactive approach to problem-solving also help ensure trial objectives are met efficiently despite the remote setup.

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

AspectRemote Clinical Trial ConsultingRemote Clinical Research Associate
CredentialsTypically requires advanced degrees (e.g., MS, PhD), industry certifications (e.g., CCRP)Usually requires a bachelor's or master's in life sciences, with some certifications (e.g., CCRP)
Work EnvironmentConsultants work remotely, providing strategic advice to sponsors or CROsRemote monitoring and site management, often working directly with trial sites
Employer & Industry UsageConsulting firms, pharmaceutical companies, CROsPharmaceutical companies, CROs, biotech firms

Remote Clinical Trial Consulting involves providing strategic, regulatory, and operational advice remotely, often to sponsors or CROs. In contrast, Remote Clinical Research Associates focus on site monitoring, data collection, and trial oversight, typically working directly with trial sites. Both roles require industry knowledge but differ in responsibilities and work scope.

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Cities with the most Remote Clinical Trial Consulting job openings:

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The most popular types of Clinical Trial Consulting jobs are:

What states have the most Remote Clinical Trial Consulting jobs?

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

Infographic showing various Remote Clinical Trial Consulting job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Remote Clinical Trial Budget Manager

Sigma Systems, Inc.

Ridgefield, CT โ€ข Remote

Full-time

Posted yesterday

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