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Medpace

Global CRO delivering full-service clinical trials

Trial Master File Specialist

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeCincinnati, OH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in a life science field is preferred.
  • Proficient knowledge of Microsoft Office and Adobe Acrobat.
  • Computer literacy, including the ability to file, scan, create folders, and organize files using various software.
  • Ability to accurately and carefully follow procedures for completing work tasks.
  • Ability to perform repetitive work without losing effectiveness or accuracy.

Responsibilities

  • Provide guidance and support to study team members and sponsors regarding Trial Master File management.
  • Initiate and manage Trial Master File 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 Trial Master File folder structures.
  • Support Clinical Trial Managers with review of Trial Master File Plans as required.
  • Support study teams during periodic Trial Master File quality checks by assisting with report development and metric reporting.
  • Report Trial Master File health to sponsors and Clinical Trial Managers.
  • Contribute to audit and inspection readiness activities by reviewing the Trial Master File, Trial Master File Specifications, and Trial Master File Plans for accuracy, consistency, and completeness.
  • Train and mentor other Trial Master File staff.
  • Help with other project responsibilities as assigned.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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