メディカル・医療/フレックスタイム制の転職求人一覧

Summary of Job Description: Grow the Parkinson’s Disease business by strengthening marketing activities and contribute to the Parkinson’s Disease patients and their caregivers.Major Responsibilities:Prepare for new product and/or new indication launch by working closely with brand team leader and brand team members.Develop, implement and manage best-in-class marketing programs utilizing digital technology to ensure successful market share growth and product sales increase for short-term and long-term.Establish and maintain relationships with KOLs, relevant organizations and other key stakeholders to develop and implement our strategyIdentify new opportunities and ways to better meet customers’ needs for short-term and long termDevelop marketing strategy with various stakeholders (in English and Japanese)Support senior brand manager for product portfolios and product life cycle plansManage to the promotional budget with the senior brand manag

ニューロサイエンス領域あるいは感染症領域における創薬研究の牽引．複数の専門部署や国内外の協業パートナーと連携し，チームメンバーを率いて創薬研究を推進． Lead drug discovery research in the field of neuroscience or infectious diseases. Leading drug discovery research by collaborating with multiple specialized departments and domestic and international collaborating partners.

• 治験の設計と実施に当たって、医学的、科学的専門知識を提供する。• 医学的および科学的専門知識を背景とした臨床的判断に基づき、開発プログラムの開発計画に戦略的提言を行う。• 安全管理部と協力して、有害事象の分析と評価を行う。• 治験におけるメディカルモニタリング。• 申請のための文書の準備の支援とレビュー。• 規制当局との会議への出席。• CROマネジメントにおける医学的、科学的観点からの支援。• プロトコル、クリニカルスタディレポートの作成支援。• 社内外の科学専門家との関係構築/維持。• 開発本部メンバーへの基礎的医学知識の共有と教育• 導入品評価のサポート• 社内の意思決定機関に対する医学的、科学的な情報の提供 • Providing scientific and medical expertise to the design and implementation of clinical studies• Providing strategic and operational guidance to teams, based on medical and scientific expertise and sound clinical judgment.• Supporting product development and research programs• Medical monitoring for clinical studies.• Assisting in the preparation and review of documents for regulatory reports. • Present clinical study outcomes and other critical data at various meetings which include but not limited to the PMDA and other regulatory authorities, academic conferences and medical congresses.• Providing medical leadership and scientifi

バイオ医薬品、ワクチン及び低分子医薬品の開発段階から承認維持管理に関するCMC薬事戦略立案，資料作成，当局対応等の業務全般を担当する． Responsible for all aspects of CMC regulatory strategy development, documentation creation, regulatory agency interactions, and maintenance management from the development stage to approval for biopharmaceuticals, vaccines, and small molecule drugs.

Role PurposeThe RLT Healthcare System (HCS) Head assumes responsibility for ensuring the readiness of the RLT Healthcare system. This includes establishing a robust imaging infrastructure, developing treatment capacity, shaping RLT policies, and strategizing partnerships. The goal is to create an advanced and forward-looking RLT treatment system that effectively supports patients who can benefit from this innovative treatment platform. The HCS Head collaborates closely with the RLT Strategy Team to develop a comprehensive plan for RLT Healthcare System readiness and leads the HCS (Healthcare System) team in building the necessary infrastructure at the account level.Major AccountabilitiesA.) Concept and lead the development of infrastructure and care processes strategies for the RLT platform• Develop a strategic healthcare readiness strategy that aligns with the Development Unit, Operations, Policy Affairs, and Value & Access. This strategy a