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. 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.

• 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;

• 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 sites
• Demonstrated organizational and prioritization skills;
• Demonstrated oral and written communication skills;
• Proficient knowledge of Microsoft Office applications.
• Bilingual Japanese and English