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 in Tokyo, 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 Build / maintain relationships with SMOs through Feasibility.Support Management in conducting/expediting feasibility activities (standalone, initial, ongoing), site selection/alignment with studies and/or therapeutic areas, and study start-up;Proactively research and understand specified site landscape/intelligence (KOL presence and knowledge, site capabilities, country standard of care and medical practices, etc.) as it relates to specific patient population, recruitment, and retention;Serve as advocate for assigned country and be cognizant of regulatory and legislative changes from a sites perspective within assigned country as well as identifying unique aspects of sites, countries that can differentiate Medpace strategies';Develop effective plans for site contacts, troubleshooting, and follow-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 organizational and prioritization skills;Demonstrated oral and written communication skills;Proficient knowledge of Microsoft Office applications.Bilingual Japanese and English Medpace OverviewMedpace 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 initiativesAwards
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.
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