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Job Overview As Biogen embarks on its first launch in a new therapeutic area, the Medical Manager, Pipeline will serve as a strategic architect and scientific leader, responsible for building the medical function from the ground up. This role offers a unique opportunity to shape
- Territory covered Cataluña and Aragon - Develop and execute an effective business plan tailored to the territory's needs. - Identify, segment, profile, and define key accounts among stakeholders such as payers, pharmacists, hospital managers, physicians, and nurses. - Build and
(Sr) Medical Science Liaison, Pipeline (f/m/d) - Northern Germany About This Role: As a (Sr) Medical Science Liaison Pipeline (f/m/d), you will be an essential field-based medical expert driving strategic scientific engagement to bolster our pipeline development in Germany. Your
The Field Excellence Lead for New Products & Account Management is the catalyst who designs the field operational launch roadmap, with a focus on the new or upgraded operational capabilities which will be critical to launch success. The immediate focus will be preparing for the L
Job Summary and Scope/Accountability The main purpose of this position is to provide field‑based medical and scientific leadership to drive medical knowledge and support informed healthcare decision‑making through high‑quality scientific exchange within the assigned territory:
As the Associate Director, Global Quality Risk Management, you will be at the forefront of Biogen’s commitment to quality excellence. Leading the charge in designing, implementing, and sustaining the enterprise Quality Risk Management (QRM) capabilities, your role is pivotal in a
Job Summary: - 規制に関する十分な知識に基づき、開発の全段階(第I相以前から市販まで)において担当するプロジェクトやプログラムの薬事戦略の策定と実施に積極的に貢献する責任を負う。 - 担当するロジェクト又はプログラムに関連し、規制当局との相談や申請業務を調整する責任を負う。 - 担当するプロジェクトに必要な日本の規制当局との会議の手配と準備を行う - 担当するプロジェクト又はプログラムの薬事的リスクを特定し、評価する。 - 薬事に対する理解を深め、プロジェクトに関わるチームに助言する 。
The Director of Rare Disease Market Access Strategy will lead development and execution of MA&R strategy for Friedreich Ataxia (FA), including the development of payer messaging, pricing & contracting strategy, coordination across all other MA&R functions, and alignment with the
Clinical Development Lead (CDL) is responsible for the overall Japan clinical development plan for assigned projects. CDL ensures studies are designed to fit Japan specific requirement and situation from clinical, regulatory, and operational perspectives. CDL is accountable for p
The Sr. Associate III, Compliance - Data Integrity is a key leadership role supporting the RTP Drug Substance Manufacturing site, with a strong focus on ensuring data integrity, compliance, and inspection readiness. This individual partners across Quality, Manufacturing, and Site
About This Role: As the Head of Quality for Device and Combination Products, you will lead the development and execution of the global quality strategy, focusing on devices and combination products. This role involves establishing cross-functional roles and serving as the primary
Job Summary : 疾患領域(TA)における科学的・教育的なメディカルサポートを、疾患領域およびバイオジェン製品に関連して、関連会社のクロスファ ンクションに提供する。 Medical Strategy and Tacticsを計画・実⾏し、必要に応じて強⼒なリーダーシップを発揮する。 TAのアソシエイトディレクターをサポートし、オフィスでのメディカル活動を⾏う。 Minimum Requirements Skills/Behaviors (refer to Career Framework) :
The PO&T Commercial Asset Development Leader is a member of the Asset Development & Portfolio Management (ADPM) team which provides cross-functional guidance across PO&T’s line functions for commercial assets. The role oversees and owns various aspects of the asset management dev
The lead of digital marketing measurement and data science is responsible for driving US business performance across digital marketing. The role will measure and analyze digital data (e.g. CRM streams, paid media, and website data) to assess promotional effectiveness, support opt
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