Medpace

Job Summary

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Associate Director, Data Management to join our Data Management team in Japan. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

• Responsible for development and maintenance of Data Management documents on assigned projects
• Represent Data Management for assigned projects in external audits (Sponsor or PMDA)
• Oversee Data Management procedures on assigned projects
• Line manage a team of Data Managers and/or Data Coordinators
• Coordinate overall data management by serving as primary contact for the sponsor, external data providers, and all project team members
• Troubleshoot and provide logical solutions to Data Management issues that arise during course of trial
• Maintain effective communication with Medpace senior management so that they are aware at all times of critical issues confronting the projects and the action plans that have been put in place to address those critical issues
• Serve as a program data management lead on multiple clinical trials

Qualifications

• Bachelor’s or Master's degree and at least 8 years clinical data management experience, including at least 5 years Data Manager experience
• At least 5 years of direct Sponsor supporting interaction
• At least 5 years of CRO or pharmaceutical company experience
• Ability to lead multiple trials
• Bilingual Japanese and English

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Hybrid work-from-home options (dependent upon position and level)
• Competitive PTO packages
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Flexible work schedule
• Competitive compensation and benefits package
• Structured career paths with opportunities for professional growth

Awards

• Recognized by Forbes as one of America's Best Mid-size Companies in 2021, 2022 and 2023
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.