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Medpace

Global CRO delivering full-service clinical trials

Data Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeTokyo, JapanNo salary listed

About the Job

Requirements

  • A bachelor's degree in a health-related field is required.
  • Strong attention to detail and working knowledge of Excel and Word are required.
  • Bilingual native or fluent Japanese and business English skills are required.

Responsibilities

  • Track case report forms.
  • Clean and update the clinical database, including generating and resolving data clarifications.
  • Reconcile clinical data.
  • Maintain study documentation.
  • Perform quality-control audits of the clinical database.

Desired Qualifications

  • One to two years of experience in a pharmaceutical or contract research organization setting is preferred.
  • Knowledge of medical terminology is preferred.

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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