M

Medpace

Global CRO delivering full-service clinical trials

Entry-Level TMF Administrator

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

About the Job

Requirements

  • An associate's degree or equivalent is required.
  • Some experience in document administration is required.
  • High attention to detail is required.
  • Strong organizational skills are required.
  • Strong written and verbal communication skills are required.
  • Knowledge of Microsoft Office is required.

Responsibilities

  • Manage the electronic filing system for trial documentation.
  • Track, maintain, and perform quality checks on electronic documents.
  • Communicate with internal associates globally regarding errors in trial documents.
  • Prepare documents for shipment.

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

Recently Posted Jobs

Explore more opportunities at Medpace

See more jobs