Clinical Research Project Coordinator

Description

• Engage in clinical trial management on a day to day level;
• Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy;
• Compile and maintain project-specific status reports;
• Interact with the Sponsor, study sites, and internal associates;
• Create and maintain project timelines; and
• Coordinate project meetings and produce quality minutes.

Qualifications

• Bachelor's or Master's degree in a health sciences field;
• Prior experience as a Study Coordinator or within the pharmaceutical industry;
• Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.
• Bilingual: fluent Japanese and English