Location: Osaka / Tokyo, Japan Industry: Pharmaceutical
Requirements:
Drives continuous improvement by streamlining operations, boosting efficiency, and exceeding client expectations.
Ensures regulatory adherence (SOPs, ICH, GCP) and timely delivery on time and budget.
Identifies scope changes, negotiates contract amendments, and optimizes project finance.
Presents at client meetings, facilitates electronic adjudication, and maintains clear team communication.
Provides study-specific training, coaching, and mentoring to enhance team performance.
Develops and maintains comprehensive trial documents (Charter, Procedures, etc.) and leads project meetings.
Requirements:
Bachelor's or advanced degree in a medical or life science field with a minimum of 8 years' experience in a similar role within the pharmaceutical industry.
Proficiency in Business-level English, both in communication and document writing is essential
Excellent understanding of the Clinical Study Process (Monitoring, Study drug handling process, Data management process).