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Remote Trial Master File Specialist Jobs (NOW HIRING)

Trial Master File Specialist

Cincinnati, OH · On-site +1

$32.25 - $44/hr

  • Medical

  • Retirement

  • PTO

The Trial Master File (TMF) is a collection of documents that stores all data and research ... In this position, you will be working with a highly experienced team of administrators, specialists ...

Clinical Trial Manager

Berkeley, CA · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

This position may be onsite, hybrid, or remote. Responsibilities: Study Management * Manage ... Maintain and oversee the Trial Master File (TMF), ensuring completeness, quality, and continuous ...

Clinical Trial Manager

Berkeley, CA · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

This position may be onsite, hybrid, or remote. Responsibilities: Study Management * Manage ... Maintain and oversee the Trial Master File (TMF), ensuring completeness, quality, and continuous ...

Oversee the core clinical portions of the Trial Master File and ensure they are up-to-date and ... May conduct on-site or remote monitoring activities as needed, including, but not limited to, Pre ...

Oversee the core clinical portions of the Trial Master File and ensure they are up-to-date and ... May conduct on-site or remote monitoring activities as needed, including, but not limited to, Pre ...

This is a remote position. This role offers the opportunity to support the planning and execution ... Maintain and organize Trial Master File (TMF) documentation. * Assist with regulatory document ...

Clinical Project Associate - Remote US

Concord, NC · On-site +1

$31.25 - $42.50/hr

This position is remote based in the US; relocation assistance and visa sponsorship are not ... You will partner with document specialist to maintain the Trial Master File (TMF) in "audit ready ...

TMF Operations Lead

OR · On-site +1

$33.50 - $45.75/hr

As our Trial Master File expert, you'll partner with Clinical Operations and cross-functional teams to build high-quality TMFs, identify and address risks early, and help ensure our studies are ...

Associate Director, TMF Operations Lead

$34.25 - $46.75/hr

Strong knowledge of Trial Master File Reference Model Structure standard and country-level ... Travel - Remote candidates must be willing to travel for company meetings for a minimum of one week ...

Sr Product File Specialist

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Product File Specialist is a key member of Sonepar's Product Data Management ... master data across assigned Sonepar Operating Companies (OpCos). The position oversees the ...

Clinical Operations Specialist (Pool)

CA · Remote

  • Medical

  • Retirement

  • PTO

... Trial Master File Management, Clinical Monitoring, Quality Assurance, Data Management and Study ... The Clinical Operations Specialist (COS) is an experienced, cross-functional clinical research ...

Clinical Research Associate (Pool)

CA · Remote

$90K - $130K/yr

  • Medical

  • Retirement

  • PTO

This position is available for remote work in the following states: AZ, CA, CO, CT, FL, GA, KS, MA ... Maintains Trial Master File (TMF)/Electronic Trial Master File (eTMF) for assigned sites. * Manages ...

TMF Operations Lead

$99K - $119K/yr

As our Trial Master File expert, you'll partner with Clinical Operations and cross-functional teams to build high-quality TMFs, identify and address risks early, and help ensure our studies are ...

Entry-Level TMF Operations Associate

Cincinnati, OH · On-site +1

$32.25 - $44/hr

  • Medical

  • Retirement

  • PTO

The Trial Master File (TMF) is a collection of documents that stores all data and research collected on a given trial. The TMF allows us to conduct a clinical trial and ensures data integrity. It is ...

Entry-Level TMF Administrator

Cincinnati, OH · On-site +1

$32.25 - $44/hr

  • Medical

  • Retirement

  • PTO

The Trial Master File (TMF) is a collection of documents that stores all data and research collected on a given trial. The TMF allows us to conduct a clinical trial and ensures data integrity. It is ...

Senior Clinical Research Associate (Pool)

CA · Remote

$120K - $145K/yr

  • Medical

  • Retirement

  • PTO

This position is available for remote work in the following states: AZ, CA, CO, FL, GA, KS, KY, MA ... Maintains Trial Master File (TMF)/Electronic Trial Master File (eTMF) for assigned sites. * Manages ...

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Remote Trial Master File Specialist information

What is a remote trial master file specialist?

A Remote Trial Master File (TMF) Specialist is a professional responsible for managing and maintaining the documentation and records related to clinical trials, typically for pharmaceutical or biotech companies, while working from a remote location. They ensure that all essential documents are complete, accurate, and compliant with regulatory standards such as Good Clinical Practice (GCP). Their work is crucial for supporting audits, inspections, and the overall integrity of clinical trial data.

What are the key skills and qualifications needed to thrive as a remote trial master file specialist?

To thrive as a Remote Trial Master File (TMF) Specialist, you need a strong understanding of clinical trial documentation, regulatory compliance, and quality management, often supported by a degree in life sciences or a related field. Familiarity with electronic TMF systems (eTMF), document management software, and Good Clinical Practice (GCP) guidelines is typically required. Attention to detail, organization, and effective communication are vital soft skills for managing large volumes of sensitive data and collaborating with cross-functional teams. These skills ensure clinical trial documentation is complete, audit-ready, and compliant with regulatory standards, which is critical for successful study outcomes.

What are the common challenges faced by a remote trial master file specialist, and how can they be addressed?

A Remote TMF Specialist often faces challenges related to maintaining document quality, ensuring timely updates, and coordinating with geographically dispersed teams. Managing secure data access and upholding regulatory compliance standards while working remotely can also be complex. These challenges can be addressed by implementing robust digital TMF systems, establishing clear communication protocols, and participating in regular cross-functional meetings to stay aligned with stakeholders. Staying proactive in learning about regulatory changes and utilizing collaboration tools can further help ensure smooth document management and compliance.

What is the difference between Remote Trial Master File Specialist vs Remote Clinical Data Coordinator?

AspectRemote Trial Master File SpecialistRemote Clinical Data Coordinator
CertificationsICH GCP, regulatory document managementICH GCP, data management certifications
Work EnvironmentClinical trial documentation, regulatory complianceData entry, database management
Industry UsagePharmaceutical, biotech, CROsPharmaceutical, biotech, CROs

The Remote Trial Master File Specialist primarily manages and maintains regulatory documents for clinical trials, ensuring compliance and proper filing. The Remote Clinical Data Coordinator focuses on managing clinical trial data, including data entry and validation. While both roles support clinical research, the Trial Master File Specialist emphasizes document management, whereas the Data Coordinator concentrates on data accuracy and database oversight.

More about Remote Trial Master File Specialist jobs

What cities are hiring for Remote Trial Master File Specialist jobs?

Cities with the most Remote Trial Master File Specialist job openings:

What are the most commonly searched types of Trial Master File Specialist jobs?

The most popular types of Trial Master File Specialist jobs are:

What states have the most Remote Trial Master File Specialist jobs?

States with the most job openings for Remote Trial Master File Specialist jobs include:

Infographic showing various Remote Trial Master File Specialist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution.

Trial Master File Specialist

Medpace, Inc.

Cincinnati, OH • On-site, Remote

$32.25 - $44/hr

Full-time

Medical, Retirement, PTO

Re-posted 22 days ago


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

13th of 73 rated research


Job description

Job Summary

We are currently hiring individuals seeking an exciting career in clinical research, managing our Trial Master File. The Trial Master File (TMF) is a collection of documents that stores all data and research collected on a given trial. The TMF allows us to conduct a clinical trial and ensures data integrity. It is an integral tool and helps teams manage trials more effectively. TMF oversight is important to the successful execution of a trial and ultimately plays a big role in a new drug or device receiving approval by the FDA. In this position, you will be working with a highly experienced team of administrators, specialists, and clinical research professionals that can help you grow your skillset while working for a growing and developing company. *This position is office-based in Cincinnati, OH. 

Responsibilities
  • Provide guidance and support to study team members and sponsors regarding TMF management;
  • Initiate and manage TMF Specifications based on scope of work, protocol, and other core documents working with functional area leads and sponsor contacts;
  • Set up and maintain study specific TMF folder structure;
  • Support CTMs with review of TMF Plans as required;
  • Support study team(s) during periodic TMF QCs by assisting with report development and metric reporting;
  • Report on TMF Health to Sponsors and CTMs;
  • Contribute to audit/inspection readiness activities by reviewing the TMF, TMF Specifications, and TMF Plans for accuracy, consistency, and completeness;
  • Train and mentor other TMF staff; and
  • help with other project and responsibilities, as assigned.
Qualifications
  • Bachelor's degree, life science field preferred
  • Proficient knowledge of Microsoft Office and Adobe Acrobat
  • Computer literacy (i.e., ability to file, scan, create folders, and organize files using various
  • software);
  • Ability to accurately and carefully follow procedures for completing work tasks; and
  • Ability to perform repetitive work without losing effectiveness/accuracy.
Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience

    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Employment Type: OTHER

What Medpace employees say

Pay

Benefits

Hours and flexibility

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992