Clinical Site Relationships Coordinator

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 Overview

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.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

 

Purpose-Driven Work

• • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

 

Collaborative Culture

• • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
  • Leadership throughout Medpace is both accessible and approachable

 

Continuous Growth & Development

• • Office based environment with on-site mentors
  • Defined career paths with clear advancement opportunities
  • Industry renowned onboarding and training programs designed to accelerate professional development
  • Ongoing training and continuous learning opportunities throughout your career
  • An environment that encourages employees to influence change, contribute ideas, and grow quickly

 

Other Employee 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 

 

Please note benefits may vary based on country. 

 

 

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

• 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;

• 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