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Remote Clinical Trial Management Systems Ctms Jobs

Veristat

Clinical Trial Manager

Charleston, WV · Remote

Flexible, inclusive culture - 70% remote workforce, 66% women-led teams * Learn more about our core ... systems including EDC, IVRS, CTMS, eTMF and other clinical project management tools required

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

Perform remote monitoring activities such as source data verification (SDV) and data entry checks ... Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.

SAB

Clinical Trial Manager, Immunology

Miami Beach, FL · Remote

Site Management: * Establish and maintain strong relationships with clinical trial sites. Provide ... Demonstrated experience using various EDC, CTMS and eTMF (Veeva, Agatha) systems. Experience with ...

BrainChild Bio

Clinical Research Associate (CRA)

Conduct remote and on-site monitoring visits in accordance with the monitoring plan, including site ... Clinical Trial Management Systems (CTMS), and vendor portals * Excellent communication ...

MUSC

... Management System (CTMS). Job Responsibilities: 30% - Analyze fully executed clinical trial agreements (CTAs) and translate contract payment terms into study team tracking system templates that ...

Fortrea

Clinical Trial Manager I- Oncology, FSP

... management strategies and ensuring compliance, including tracking within applicable systems ... CTMS, eTMF, and vendor platforms (e.g. Veeva Vault, Medidata). * Effective leadership in remote and ...

Fortrea

... management strategies and ensuring compliance, including tracking within applicable systems ... CTMS, eTMF, and vendor platforms (e.g. Veeva Vault, Medidata). * Effective leadership in remote and ...

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How much do remote clinical trial management systems ctms jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for remote clinical trial management systems ctms in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What is the difference between Remote Clinical Trial Management Systems Ctms vs Clinical Data Coordinators?

AspectRemote Clinical Trial Management Systems (CTMS)Clinical Data Coordinators
Primary RoleManage and oversee clinical trial operations using specialized softwareCollect, clean, and manage clinical trial data
Required SkillsKnowledge of CTMS software, project management, regulatory complianceData management, database tools, attention to detail
Work EnvironmentRemote or office-based, often within pharmaceutical or biotech companiesTypically office-based, within clinical research settings
CertificationsOften requires clinical research or project management certificationsRelevant certifications in clinical data management or related fields

While both roles support clinical trials, Remote Clinical Trial Management Systems (CTMS) professionals focus on managing trial operations through specialized software, whereas Clinical Data Coordinators handle the data collection and quality assurance aspects of trials. Both roles are essential in the clinical research process but differ in their core responsibilities and skill sets.

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Remote Clinical Trial Management Systems Ctms jobs near you
Infographic showing various Remote Clinical Trial Management Systems Ctms job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Clinical Trial Manager

Veristat

Charleston, WV • Remote

Full-time

Medical, Retirement

Posted 13 days ago

Job description

Job Description:

Clinical Trial Manager

The Clinical Trial Manager (CTM) provides operational expertise and leadership to multiple clinical trial teams, to ensure the effective and efficient delivery of all aspects of multiple studies, through all phases of clinical study management, in accordance with applicable Veristat Policies, Standard Operating Procedures (SOPs), conventions and instructions, as well as current Good Clinical Practice (GCP), International Conference on Harmonization (ICH), and applicable local regulations.

Make an Impact at Veristat!

Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.

  • 105+ approved therapies for marketing applications prepared by Veristat
  • 480+ oncology projects in the past 5 years
  • 350+ rare disease projects delivered in the past 5 years
  • Flexible, inclusive culture - 70% remote workforce, 66% women-led teams
  • Learn more about our core values here!

What we offer:

The estimated hiring range for this role is $150K - 160K plus applicable bonus. This hiring range is specific to the USA and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.

  • Benefits vary by location and may include:
    • Remote working
    • Flexible time off
    • Paid holidays
    • Medical insurance
    • Tuition reimbursement
    • Retirement plans

What we look for

  • Bachelor's Degree required; degrees in health sciences strongly preferred

  • 5 or more years of experience as a CRA in a CRO or Pharmaceutical setting, and ability to effectively lead a project team required

  • Thorough knowledge of clinical operations, clinical development process, and ICH/GCP and regulatory environment required

  • Ability to serve as a mentor, coach and trainer for assigned CRAs

  • Excellent oral and written communication skills in English, including proficient presentation skills required to effectively support and manage exchanges with external customers; ability to speak and write in other languages a plus

  • Proficient knowledge of study specific therapeutic area to enable appropriate input to study documents (e.g., protocols, CRFs, EDC development)

  • Proficiency in Microsoft Outlook, Word, Excel, and PowerPoint required

  • Proficiency in, and ability to learn new, clinical systems including EDC, IVRS, CTMS, eTMF and other clinical project management tools required

  • Ability to self-motivate, be a team player, and work independently

  • Excellent critical thinking and problem-solving skills required

  • Ability to self-motivate, work collaboratively within a team, proactively manage workload, and manage competing priorities in a fast-paced environment required

Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.

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Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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