· メディカルエデュケーション&コミュニケーション部スタッフ · FAQの作成 · ローカルレスポンスドキュメント(LRD)の作成 · コールセンターの運営 · 2次エスカレーション対応 · グローバル質問対応管理サイト(One GMIの管理) · . FAQシステムの構築(外部サイト、社内Webページなど). 外部ベンダー管理 Li. ...

The Medical Education Specialist will drive regional medical education strategy and digital transformation across Japan. The Specialist will coordinate clinical education activities, deliver medical education events in line with strategic responsibilities. · ...

The Medical Information Specialist will collect medical/scientific information regarding company products and respond promptly to inquiries and requests from internal and external stakeholders. · ...

The medical device regulatory affairs specialist role involves ensuring compliance with regulatory requirements for medical devices. The position entails creating and submitting application materials to relevant authorities, · advising on PMDA matters including face-to-face consu ...

アンメットメディカルニーズに応えるエビデンス創出、ならびに医科学専門家との医学的・科学的議論を通じ、医療環境向上に貢献し、かつ、患者とその家族、医療従事者にとっての製品の価値を最大化する。 · ...

+Clinical Research Specialist · 治験、市販後臨床研究および市販後調査の計画・実施・進捗管理と報告書作成 · ,担当施設における手続き業務、モニタリングならびに監査対応 · ,関連文書の作成および確認 · ,内部・外部関係者との良好な関係構築 · ,, · ...

Roles providing expertise on scientific topics regarding relevant disease areas and Company assets to ensure their safe and appropriate use by patients. · Acts as a field-based expert, building relationships with External Experts as trusted scientific partners. Exchanges credible ...

This position will be involved in HRM operations with a focus on overall Compensation & Benefit operations and HRIS management system data maintenance and specification changes. · ...

· Medical & scientific subject matter expert for assigned Disease Area (eg: dermatology, rheumatology) Generate medical and scientific evidence to fulfill unmet medical needs through utilization of RWD/RWE Transversally collaborate with other functions locally and globally to he ...

The Cell Therapy Scheduling and Logistics Specialist I will be responsible for scheduling and monitoring patient treatment schedules for the manufacturing of Celgene's autologous cellular immunotherapy products. · Responsibilities include:Coordinate with cell collection centers t ...

This position will be involved in HRM operations with a focus on overall compensation benefit operations and HRIS data maintenance and specification changes. · C&B related setting up job profiles responding to changes in the compensation system maintaining job descriptions partic ...

The Medical Science Liaison (MSL) role involves exhibiting scientific and clinical knowledge to facilitate timely and appropriate exchanges with influential external experts. · Exhibits strong knowledge of relevant diseases, healthcare environment, competitors; can articulate med ...

No resume provided. · Supply Chain Senior Specialist. · ...

This position will be responsible for all compensation and benefits operations as well as HR system support. · The position will be responsible for compensation system changes planning and operations and will be expected to work as a specialist in compensation benefits and labor ...

The Safety Specialist collaborates with teams to ensure safety communication and product stewardship. · ...

This is a Medical Science Liaison role for the dermatology area. · We are looking for an individual with strong scientific knowledge and leadership skills. · ...

Supports identification and collection of competitive technical product information and provides market-specific claims merchandising information demos and practices for current generation benchmark products.

Provides Japanese Labelling & Artwork Regulatory expertise across a Therapeutic business unit. Delivers strategic and operational regulatory input and guidance to the cross functional teams. · Creation, update and maintenance of the Japanese package inserts in line with the CCDS, ...

The Japan Sr Project Lead serves as the project leader for development pipelines with comprehensive responsibilities including end-to-end development strategy alignment at both local and global levels. · ...

Clinical Science Lead also known as Sr Clinical Scientist responsible for leading regional country level Development Team in matrix setting ensure alignment across key stakeholders promote team work drive development Clinical Development Plan CDP relevant study designs team effor ...

Clinical trial experience is required of MDs with over 3-5 years of corporate experience and development experience who hold Japanese medical licenses. · ...