Welcome page Returning Candidate? Log back in! Site Relationships Coordinator Job Locations Japan-Tokyo Category Clinical Trial Management Job Summary

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Site Relationships Coordinator to join our Clinical Trial Management team. 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 Provide oversight of preferred site relationships within assigned countries;Provide ongoing support of sites, including identifying and discussing future new business opportunities and feasibility assessments;Develop effective plans for site contact and follow-up;Serve as main point of contact for project teams regarding site performance issues and updates on pertinent site information;Support management in expediting feasibility, site selection and study start-up; Qualifications Bachelor's degree and at least 2 years of Clinical Monitoring experience;Knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines;Demonstrated ability to effectively communicate with internal and external parties, including Principal Investigators and consultants;Possess a thorough understanding of feasibility assessments, strategies, approaches and requirements in order to facilitate these processes;Demonstrated ability to manage complex/high priority site relationship tasks, including relations with partner sitesDemonstrated organizational and prioritization skills;Demonstrated oral and written communication skills;Proficient knowledge of Microsoft Office applications.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 6,000 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

Flexible work environment Competitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation events Employee health and wellness initiatives

Awards

Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024Continually 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.

 

EO/AA Employer M/F/Disability/Vets

Connect With Us! Not ready to apply? Connect with us for general consideration.