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新着求人 プロダクトマネージャー  (MPM-22)
募集職種 外資系製薬メーカーの Scientific Communications, Manager
勤務地 全国
会社概要 非公開
求人要件 雇用形態:フルタイム  社員区分:正社員 部門:オンコロジー
Responsible for all aspects of scientific communications and play a role of communication leader for assigned Oncology product
Major Accountabilities
•Lead publication strategy, planning and execution for assigned projects
•Coordinate medical education strategy, planning and execution to ensure awareness of key data and key messages for ** products to internal and external stakeholders
•Drive a new medical expert engagement model with a strategic disease focus by implementation of BUILD (e.g. digital engagement, preceptorship, new congress model) and innovation beyond
•Lead activities for congress scientific communications across disease areas and products
•Prepare and maintain timely high quality delivery of congress scientific communications, publications, slide kits, advisory board materials, etc.
•Perform appropriate slide review for ** sponsored symposium
•Build strong working relationships and actively collaborate with key internal and external stakeholders (LF heads of OMA and GDD, JPTs, IDAPS teams, legal/regulatory/compliance, global Sci Comm, medical experts, consultants, and professional societies)
•Lead all aspects of publication and medical education agencies in support of scientific communications. Identify and screen appropriate vendors, solicit, evaluate and approve proposals in collaboration with sourcing
•Compliant with all legal regulatory and ** requirements for scientific communications (publications and medical education materials)
•Advocate continuous improvement of quality
•Comply with company standards and local regulations
•Ensure adequate reporting of adverse events / technical complaint / compliance issue in accordance with company procedures
•100% timely delivery of all training requirements including compliance and oversee compliance with SOPs, related instructions
Education:Advance degree in life science/healthcare
Experience/Professional requirement:
•> 5 years of experience in relevant function of the pharmaceutical industry and publication/education experiences are preferred
•Basic knowledge of clinical trials or experience of educational event
•Basic knowledge of project management and budget management
•Thorough knowledge of regulations
Languages:Fluent Japanese and intermediate English (oral and written)
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