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Medpace

Global CRO delivering full-service clinical trials

Associate Director/Director - Site Contracts

Contract ManagementConfirmed live in the last 24 hours
Full-timeTokyo, Japan

About the Job

Requirements

  • A bachelor's degree is required.
  • At least 8 years of contract management experience in clinical research is required.
  • Experience managing a group is required.
  • Fluency in Japanese and English is required.
  • Excellent communication, negotiation, and leadership skills are required.

Responsibilities

  • Lead the Site Contracts team throughout the Study Start-Up Process.
  • Develop the group strategically, manage the team, and continuously improve processes.
  • Provide input on new business development opportunities.
  • Develop and maintain relationships with clients.
  • Guide and support staff negotiating site contracts and budgets.

Desired Qualifications

  • Experience in a contract research organization is preferred.
  • A general understanding of study start-up and how site contracts integrate with other clinical operations functions 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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