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About the Role
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 and maintain relationships with SMOs through Feasibility.
- Support Management in conducting/expediting feasibility activities, site selection/alignment with studies and/or therapeutic areas, and study start-up.
- Proactively research and understand specified site landscape/intelligence 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.
- Develop effective plans for site contacts, troubleshooting, and follow-up.
Requirements
- 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.
- Demonstrated organizational and prioritization skills.
- Demonstrated oral and written communication skills.
- Proficient knowledge of Microsoft Office applications.
- Bilingual Japanese and English.
Location
- Tokyo, Japan
Work Type
- Full-time
- Office-based
Experience Level
- 2 years of Clinical Monitoring experience
Education Level
- Bachelor's degree
Benefits
- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events
About the Company
- Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research.
- We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective.
- Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.