社名非公開/IT マネージャー ビジネスアナリスト(ディジタルプロダクトライン)の求人【バイオ転職ナビ】


IT マネージャー ビジネスアナリスト(ディジタルプロダクトライン)  /  社名非公開

職種 IT マネージャー ビジネスアナリスト(ディジタルプロダクトライン)
社名 社名非公開
業務内容 This company discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases. What matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found. The IT Manager, Business Analyst for Digital PLO will be based in Japan and will report into the Regional Digital PLO Lead. The Digital product line organisation has an Asia Pacific regional focus with 2 primary platform responsibilities; ・ Digital eco-system, that includes websites, mobile applications, multi-channel (email, webinars) engagements, content management and hosting platforms. ・ User Productivity & Collaboration solutions with a focus on innovative ways of working using cloud, mobile, video and social technologies. The position will work closely with the Product Line Leader, regional BTLs (Business Technology Leaders), BPO, EA & shared services teams to evolve the product line to meet business strategic objectives. Additionally, the person will be responsible for overseeing delivery of business technology projects, requirements gathering, release planning and technical application life cycle management. Primary Duties & Responsibilities ・ Be a technology partner, working with business partners to identify unmet needs, propose IT solutions, and assist management in the development of business cases and project charters ・ Cultivate relationships with external agencies, partners, J&J suppliers and customers, to develop deep insights into the needs of our business departments, patients, customers, markets and communities and become the go-to person for our business / technology partners. ・ Lead the technical discovery process for Digital and Productivity projects, scoping needs, gathering requirements and producing functional specifications for a solution build, based on regional and global standards ・ Conduct Business Analysis: Map out business process; Capture business requirements and specifications (story boards, use cases); support translation into technical requirements. ・ Support continuous process improvement; mapping current and future state, root ……(以下詳細は面談時にご案内します)
求める経験 ■Qualifications ・Bachelor’s degree with at least 6 years of relevant experience ・Strong knowledge of platforms and technologies comprising the digital ecosystem (e.g. static/dynamic web, mobile apps, campaign email, hosting approaches, media and content management systems) ・Experience of HealthCare solutions for engaging Doctors, Careers or Patients through digital channels is highly desired ・Knowledge of platforms and technologies within the Productivity & Collaboration domain, this includes latest Microsoft O365, enterprise social apps, messaging, video or chat tools as well as single device solutions ・Knowledge of supporting Commercial Domains such as CRM (Veeva, SFDC), data analytics will be highly regarded ・Ability to relate business priorities to associated technology investments is required. ・Ability to recommend priorities to multiple stakeholders based on the highest business value is required. ・Knowledge of trends in technology and opportunities in healthcare is preferred. ・Proven track record of successful project delivery with a complex, global organization is required. ・Broad technology experience with ability to lead assessments of proposed solutions and develop recommendations is required. ・Understanding of the business impact of different solutions and ability to assess impact and communicate the tradeoffs between business needs, technology requirements, timelines, costs and risks is required. ・Experience with the management of budgets and allocating resources accordingly is preferred. ・Good understanding of Agile with ability to coach/mentor IT and business partners is preferred. ・Working knowledge of SDLC and rRDM including requirements elicitation, system design, development and validation/regulatory requirements. ・Experience working in process-driven environments (SDLC, Agile) co-ordinating internal and external delivery partners toward a single goal ・Certification in Business Analysis (e.g. ISEB Business Analysis Diploma) and Project Management (e.g. PRINCE2, APMP) areas highly regarded
語学力 英語力:中級
年収 900万円 - 1300万円
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



IT マネージャー ビジネスアナリスト(ディジタルプロダクトライン)と似た条件の案件を探す

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**武田薬品の長期収載品(LLP)を担当して頂きます** 医薬品並びに医療機器の製造販売業における品質保証業務(GQP)について、所属グループの計画を策定して遂行する。 ・国内外の製造所の管理監督(市場出荷判定の委託、取決め、監査など) ・変更、逸脱、苦情などの品質情報の処理、品質不良等の重大な品質トラブルの問題解決と措置(自主回収等) ・行政査察の対応(業許可更新等のGQP査察、海外製造所のGMP適合性調査の同行) ・品質システムの構築(国内レギュレーションとグローバルのポリシーと基準書に基づく体制の構築とSOPの制定) ・製品ライフサイクルを通した品質保証の構築 ・教育プログラムの充実と人材育成


-KOLマネージメント(外勤ベース) -医学的、科学的見識に基づいた情報の提供と収集 -メディカルプランの作成と実行 -研究者主導試験のサポート

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)