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Remote Clinical Trial Operations Jobs (NOW HIRING)

Vitalief

Clinical Trials Coverage Analyst

Chicago, IL · Remote

$70K - $85K/yr

... fully remote capacity, supporting a leading academic clinical research center in Chicago. The ideal candidate brings strong expertise in Medicare billing guidelines, clinical trial operations ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... Operations. Requirements To be successful you will possess: * A degree in life sciences or nursing ...

Allucent

Clinical Trial Lead

Cary, NC · Remote

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... Operations. Requirements To be successful you will possess: * A degree in life sciences or nursing ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... Operations. Requirements To be successful you will possess: * A degree in life sciences or nursing ...

ICON

Clinical Trial Manager

Raleigh, NC · On-site +1

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Manage the day-to-day operations of assigned trials and responsibilities to ensure completion per ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

The successful candidate will manage members of the clinical operations team, including those at ... Perform clinical research site activities, which can include onsite or remote monitoring, co ...

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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 Aug 12, 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.

More about Remote Clinical Trial Operations jobs
What cities are hiring for Remote Clinical Trial Operations jobs? Cities with the most Remote Clinical Trial Operations job openings:
What are the most commonly searched types of Clinical Trial Operations jobs? The most popular types of Clinical Trial Operations jobs are:
What states have the most Remote Clinical Trial Operations jobs? States with the most job openings for Remote Clinical Trial Operations jobs include:
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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 86% Full Time, 11% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Senior Clinical Trial Manager (CTM)

Praxis Precision Medicines, Inc.

OR • On-site, Remote

Full-time

Re-posted 6 days ago

Job description

Senior Clinical Trial Manager (CTM) 

Location:   This position may be performed remotely with travel to the Boston area as needed.   

Position Summary 

This role will be responsible for project management in the initiation, execution and close out of domestic and international clinical studies, including study concept and design, feasibility assessments, study start-up, contract and budget oversight, data exchange and support of data analysis and interpretation. 

This position requires both the knowledge and experience to work within established clinical trial paradigms while exploring and embracing new approaches to conducting research to support data aggregation and analysis to advance patient care. The Sr. CTM will participate on clinical project teams to achieve quality results in a cost-effective and timely manner. S/he will be a key team member to establish key practices and procedures for the clinical team. 

Primary Responsibilities 

  • Manage study activities in the successful execution of clinical trials from protocol concept to clinical study report, complying with Good Clinical Practice (GCP) guidelines and international regulations 
  • Manage strategic engagement with key collaborators 
  • Set-up and oversee clinical trial-related trackers such as regulatory documents, trial master file (TMF), startup progress, screening/enrollment, study invoices/payments, project budgets, etc. 
  • Key contributor to IRB/EC and regulatory submissions 
  • Oversee TMF reviews to ensure completeness and inspection readiness 
  • Regularly review documents to ensure adherence to Clinical Operations and/or project specific quality requirements (e.g. SOPs, work practices, training guides) 
  • Identify and mitigate against study risks, escalating as necessary 
  • Direct initiatives to identify and implement best practices and continuous improvement plans in clinical development 

Education and Professional Experience 

  • Bachelor's degree in a scientific field required; advanced scientific degree a plus 
  • 5+ years directly managing clinical trials in Sponsor or CRO setting 
  • In-depth knowledge of clinical trial operations, ICH, GCP Guidelines and other applicable regulatory requirements 
  • Experience directing members of clinical operations teams 
  • Experience working in a team across multiple functional areas (e.g., Quality Assurance, Data Management, Biostats, Medical Writing, Safety, Clinical Supply, Finance) 

Other Essentials and Key Success Factors 

  • Intellectual curiosity, innovation and creative problem solving with an entrepreneurial spirit 
  • Ability to think critically in fast-paced projects with a keen sense of urgency and demonstrated ability to problem solve 
  • Self-motivated and able to work autonomously, as well as a member of a collaborative team 
  • Highly-organized and detail-oriented with a passion to deliver quality results 
  • Strong verbal and written communication skills with an ability to build relationships internally and externally 
  • Highest levels of professionalism, confidence, personal values and ethical standards 

Apply