- 非公開 No.AS200106
- ・Accountable and responsible for development and implementation of medical development plan on complex programs resulting in quality regulatory submissions.
・He/she serves as a medical lead in multi-desciplinary teams, acts as an interface with discovery teams through regulatory authorities and commertial organizations, and chairs the global clinical team meetings.
・Recent (within 3 years) experience in a similar position at a pharma company for more than 2 years.
・Experience in designing Phase 2 or 3 clinical trials, writing trial protocols, and executing clinical trials.
・Maintein personal or professional relationships with influential world key science leaders.
・Fluent in English (preferably but not mandatory in Japanese also) and regularly chairs international meetings.