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Medpace

Global CRO delivering full-service clinical trials

Associate Director/Director - Clinical Monitoring

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

About the Job

Requirements

  • A bachelor's degree.
  • 10+ years of CRO or pharmaceutical industry experience in Clinical Monitoring, including 4+ years as a CRA and 6+ years as a CRA Manager; this experience is preferred.
  • Advanced knowledge of Good Clinical Practice and J-GCP.
  • Strong leadership, mentoring, and motivational skills.
  • Effective written and verbal communication skills in English.
  • Proficient knowledge of Microsoft Office software.

Responsibilities

  • Directly supervise CRA management to ensure effective line management.
  • Oversee CRA resourcing and allocation across studies and sites.
  • Participate in planning Clinical Monitoring recruitment and retention strategies.
  • Oversee effective CRA Manager training and oversight strategies.
  • Support global and local management of Clinical Monitoring operational metrics and goals in Japan.

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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