仕事内容Lillyは、世界中の人々のより豊かな人生のため、革新的医薬品に思いやりを込めて届けます。Lillyは、インディアナ州のインディアナポリスに本社を置く世界的なヘルスケア企業です。世界中にいる同社の人の社員は、画期的な新薬を発見して、それを必要とする人々に届けること、疾病の理解と管理を改善すること、そして慈善活動およびボランティア活動を通じたコミュニティへの還元のために働いています。同社は仕事に最善を尽くすと共に、人を第一に考えています。同社は世界中の人々の人生をより良くしたいと強く思っている人を探しています。
Job Description
The purpose of Pharmaceutical Project Management (PPM) role is to have overall responsibilities for working with the leadership of the Global counterparts and the corresponding Affiliate Business Unit functions to assure development and implementation of appropriate pharmaceutical development strategies and plans from early-phase to end of the lifecycle of the molecule on time and on budget in the relevant therapeutic area. The key deliverables are full portfolio coverage, simultaneous development and launches, and creating value across the entire product life stage. The role will be assigned to one or multiple Therapeutic Areas (Immunology, Neuroscience, DOCTA/CMH or Oncology).
[1] Align the Portfolio, Development to BU Strategies
Engage Medical, Clinical, Regulatory, CMC/Manufacturing, Marketing, Safety Functions and other functions to deliver the portfolio and align drug development strategies with BU strategies.
Provide leadership for development of Product Lifecycle Plan in alignment with the Therapeutic Area development and commercial strategies.
Deliver necessary information and data about the new/ongoing projects for the portfolio and business plan management.
[2] Lead Value Maximization Through Product Lifecycle
Lead to develop robust Japan Project Plan that fortifies linkages to Asset Profile, Value proposition, MMFA (Manufactured Marketed Forms Agreement) and scope, assures quality and consistency of content, and translates into operational objectives.
Translate Japan marketing, medical and regulatory needs for the molecule/new indication/line extension (including new formulation / delivery solution) into the global integrated plan.
Lead overall launch readiness and co-lead the affiliate overall launch readiness in collaboration with respective commercial leader.
Ensure post-marketing activities including issue management are managed well by providing leadership to cross-functional collaboration.
[3] Deliver Results
Lead the team to meet or exceed overall project goals (completion of clinical studies, CMC deliverables and NDA/device preparation, submission and approval timing, etc.)
Deliver project milestones on time, on budget, within scope, and to high quality standards by holding functions accountable for achievement of key project deliverables in alignment with the agreed to project plan and in compliance with Japan quality standards.
Identify areas for where process improvement will enable better results and work with discipline leaders to impact change.
[4] Apply Project Management Knowledge and Processes
Work with Japan governance to authorize project scope and plans. Scope and plans should be based on broad scenario planning, robust risk management planning, and reliable execution (timeline, FTE, and budget) planning which ensures all functional requirements are appropriately reflected.
Develop and implement stakeholder, global, and team communication plan to ensure alignment with medical affairs strategy and product development strategy. Lead external communication strategy related to development (e.g. data read outs, regulatory outcomes). Provide rapid and quality responses to external customers.
Monitor and control performance of the overall project that utilizes appropriate tools and techniques (project systems, budget: plan vs. actual, FTE: plan vs. actual, etc.), and ensure change management process is in place to manage scope and plan.
[5] Build Winning Culture Through Effective People Management
Coach team members by providing timely constructive feedback and recognition to good results and behaviors.
Create an environment that encourages intelligent risk taking and fosters wining culture within the team.
Support the growth of project management expertise in Lilly Japan through participation in shared learning forums, staff meetings and training programs.
経験・資格●Knowledge and Skills
●Education and Work Experience Desirable to Perform Role:
●Additional Preferences
勤務地
想定年収
福利厚生・待遇
勤務条件【勤務時間】8：45～17：30
【清算制フレックス勤務】適応あり。フレキシブルタイム：5時～22時内で勤務。(ただし、一斉休憩を除く)1日の必要最低労働時間：4時間(半日休暇時は2時間)一斉休憩：12時～13時
【在宅勤務制度】有
完全週休2日制（土・日曜日）、祝日、クリスマス、年末年始・夏期※年間休日125日 年次有給休暇、慶弔等
6か月間
試用期間中での賃金の違いはございません。
昇給年1回、賞与年3回
保険（雇用・労災・健康・厚生年金保険）
Recruiting No.
社名
事業内容
【東証プライム上場 財閥系 海運会社】 事務系総合職
【東証プライム上場 財閥系 総合商社】 エネルギー部門 次世代燃料チーム：バイオ燃料・次世代液体燃料市場の分析、トレーディング戦略の策定
【東証プライム上場 日本を代表する総合重工業メーカー】 社内SE（クラウドサービス基盤の構築・運用を担うインフラエンジニア）
多くの人が待ち望み、誰も作れなかった新薬を高度な技術で生産し、世界市場に届けます。
医師が安心して意見交換できる会員制サイト『MedPeer』。臨床の「集合知」が新しい価値を生み、ビジネス拡大中です。
「ODMメーカー」として、業界の中で独自の事業展開をしていこうとしています。
真摯で熱い気持ちを持ったメンバーが揃っている会社です
相手と意思疎通を図る、何かしらのツールを持っていて欲しい
