大手製薬メーカー/Project Manager (R&D)の求人【バイオ転職ナビ】


Project Manager (R&D) 急募求人  /  大手製薬メーカー

職種 Project Manager (R&D)
社名 大手製薬メーカー
業務内容 <Description> Ensure the project management in alignment with the established organizational objectives ●Project planning management ・Manage to build the Japan development plan in collaboration with Japan and global development teams and other stakeholders ・Lead the project team to obtain the endorsement from governance body in timely manner ●Timeline management ・Develop an appropriate project timeline on the IT system taking into account the strategy and plan of the project ・Provide the oversight of the project status through tracking milestones and flag up any critical delay for mitigation purposes ●Issue /risk management ・Develop and maintain issue / risk management plans including solution plans ・Upon being alerted of impending issue / risk, design a recovery plan ・Facilitate Lessons & Learned exercise in the team at key stage gates ●Project Budget Management ・Manage, review and challenge the project budget plan (single year budget plan & multiple years of the cost to launch) ・Track the project related expense and manage updates when required ・Generate project resource information using IT system ●Communication and collaboration ・Facilitate and coordinate the core project planning discussion to make the team move toward project’s goal ・Collaborate with global organization such as global PMO (project management organization) proactively to proceed project from perspective of global and Japan interest
求める経験 <REQUIRED> ・A bachelor degree; life sciences, engineering, or business management specialization is preferred ・At least 3 years experience in project management and/or team leadership, functional line management in one or more of the Pharmaceutical R&D functions ・Experience of managing or leading global or multi-country project ・Ability to partner with people at all levels of the organization ・Ability to respond flexibly to changing project priorities and work assignments. ・Ability to influence and negotiate without specific authority. Interpersonal skills and Change Agent - Excellent interpersonal skills, with the ability to build relationships, act as a change agent, and adapt to rapidly changing organizational and business issues ・Strong analytical skills with high IT literacy in Excel, Power Points, other database ・Experience to ensure the business complies with all legal legislations through compliance with the highest standards of pharmaceutical industry propriety ・Experience to assure business compliance and control within the Health Care Compliance obligations, Sarbanes Oxley and other audit requirements ・Strong English communication skills (Janssen Japan R&D project managers work with global teams) <PREFERRED> ・Experience of clinical development or regulatory affairs ・Professional project management certification and/or diploma (PMP) ・Proffesional business management certification and/or diploma ・Innovative Thinking and Approach - Capable of identifying, adapting, and applying innovative and creative methodologies that will allow to build an optimal PM support-environment
語学力 英語力:中級
年収 800万円 - 1400万円
雇用形態 正社員(期間の定めなし)











  • 人気企業(大手企業・優良企業)や人気業種
  • IPO要員や新規事業立ち上げなど重要度なポジション



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Clinical Programs Lead LOC

<Summary> This section focuses on the main purpose of the job in one to four sentences. -The primary responsibility is to be the lead for all Local Country (LOC) study activities ( in JP PMS activities led by the GPSP person are out of scope) ) in Japan. This role in Japan is expected to oversee study activities related to global programs which JP joins (regardless international or local stand-alone study) and contribute to the global dossier.This role should contribute to the understanding of the JP needs and feed this information to the global CPM.The role holder assures the country Medical Affairs plans are visible to the global CD and CDO groups in a timely manner.The position holder is expected to drive communication between the local and global functions, guide on required processes and structure if there is a special need for a role, assure alignment with the compound/development and outsourcing strategy, support oversight of the selected vendor, drive appropriate quality of the local studies and work in closest collaboration with the global Program CDO representative aligned with the predefined RACI by giving input onto R&R for each study. -Close collaboration and communication between stakeholders i.e. Drug Safety and Risk Management , Regulatory Affairs, MA, Patient Outcome, Clinical Development, Clinical Quality, External Partnerships and the CDO functions is expected. -In Japan the role holder should support local RA with input into the development activities as needed, especially for JP stand-alone studies and support communication with the global teams. This is a focus of this role. -Dependent on the stage of the life cycle of a compound the scope of oversight (of study and strategy) and interactions may vary. <Essential Duties and Responsibilities> This section contains a list of five to eight primary responsibilities of this role that account for 5% or more of the work. The incumbent will perform other duties assigned. ・Represent Clinical Development Operations (biostatistics, data management, clinical operations, and clinical scientific writing, outsourcing) on brand planning meetings and respective CD activities to support realistic budget, time, allocations. ・Assure full transparency of local studies to the global organization and work closely with the respective global functions. ・Works collaboratively with the GPSP representative and global program lead ・Provides input to ……(以下詳細は面談時にご案内します)