掲載期間:25/07/11~26/01/10 求人管理No.027103

新着 外資製薬メーカー

プログラムマネージャー/ノンラインマネージャー /オンコロジー・免疫領域事業本部

  • 新着求人
  • 英語を活かす

※こちらに入力した項目が企業に直接届くことはございません。


募集要項

大手外資製薬メーカーにてプログラムマネージャーをご担当いたただきます。

仕事内容

Accountabilities
Accountable for translating asset strategy into actionable plans. Guides team to develop integrated program plan and budget ensuring alignment of the project strategy with operational delivery; holds team accountable to plan. Ensures Global input from Japan in particular for early assets.
For the digital assets orchestrates the entire development and commercialization process of the digital health asset from ideation to full commercialization and subsequent maintenance

Responsible for documenting the asset strategy, key decisions and roadmap and ensures the information is up-to-date and consistent.
Ensures that the Asset Evidence Plan (AEP)and/or Integrated Evidence Plan (IEP) and/or the Target Product Profile (TPP) reflect Japan development strategy for the product milestone releases at the Human Pharma Leadership Committee (HPLC).
For Regional Input from Japan, including early assets (between SOD and PoCP), coordinates with Early Evidence Lead and supports TA Head.
Holds the team accountable to their commitments and organizes necessary follow ups and deployment of necessary knowledge and resources.
For digital assets, ensures that goals, scope, and product domain are understood by all team members and relevant stakeholders.

Responsible for the seamless execution of program deliverables and related activities; escalates delays to asset lead and respective teams. Ensures proactive identification of risks, backlogs, deviations and compliance topics, working with asset team members in their respective areas, and brings team members together to develop recommendations and risk mitigation plans

Supports Asset Lead in coordinating interactions with leadership committees, orchestrates the team to develop cohesive input into governance meetings and to prepare milestone release documentation; maintains repository of governance presentations/decisions.
Coordinates and facilitates senior management presentations, interactions, and documentation
Documents and tracks program-level agreements (e.g alliance, in-licensing contracts, etc), maintains repository of key program documents and logs, including information on partners, collaborators

Manages at operational level critical interfaces among different leads, and other functions/parties not represented in the asset team.
Enables the cross-functional team to achieve jointly defined timelines and milestones and coordinates joint cross-teams (e.g. between Value and Evidence teams) and cross-functional (e.g. submission) deliverables, troubleshooting issues, documenting actions and tracking progress, timelines and costs

In collaboration with the Asset Team members: manages the project plan including timelines and interdependencies between the studies

Serves as the interface and provides input into TA and xTA portfolio planning and coordination, including project classification and characteristics, critical path, timelines and cross-functional resource implications.
For the Digital assets, serves as a strong collaboration partner with /Digital Innovation and other functions to coordinate and align platforms and processes.

Coordinates asset team meetings, documents agenda/minutes, tracks open issues until closure and communicates key decisions to accountable stakeholders outside of asset team if applicable.
Relentlessly drives prioritization, efficiency and speed and facilitates team's agile ways of working (i.e. sprint planning, daily stand-ups, retrospectives etc.)

Regulatory and / or Organisational Requirements
Act at all times within local and global governance standards and facilitate compliance to pharmaceutical standards/ethics/rules via his/her decisions.
Follow all company procedures and processes with respect to Quality, Finance, HR, IT, Legal & Compliance etc.

Job Complexity
The role of Program Manager will handle multiple interfaces and deliverables of drug development process within an asset team and associated next-level teams spanning from early to late stage, from clinical to commercial and managing complex cross-functional deliverables e.g. milestone release, submission and launch preparation. The incumbent needs to be able to reconcile diverging perspectives into a consolidated, ambitious and feasible plan and proactively manage interdependencies and risks in its execution.
For the Digital assets, the PM works in a cross-functional matrix environment of very high complexity including a wide variety of different subject matter experts within the digital health asset team and enabling functions resulting in demanding stakeholder management.

Interfaces
Mainly the Asset Team leads (Asset Lead, Evidence Lead, Value Lead etc.)and next level teams. Key decision making bodies/commitees such as the TALC; Program Managers of other Asset Teams.
For the digital Assets the role has major interfaces with the asset technical development team, ,Group Functions, external partners, patients, and stakeholders.

Job Expertise
Solid experience and track record in process management, project management and delivering within agreed time, cost and quality.
Appreciation of the complex nature of product (drug and digital) development processes and familiarity with key processes and stages of product (drug and digital) development. Experience in agile working methods and know-how on bridging agile and traditional ways of working.

Job Impact
Being part of an asset team, the Program Manager plays a crucial role in delivering successful products in portfolio of patients solutions. Working closely with the Asset lead (and/or Early Evidence Lead), the PM provides oversight of key deliverables, interfaces and significant budget and is instrumental for success of an Asset team.

仕事内容(変更の範囲)

会社の定める業務

応募条件
【必須事項】
・Advanced degree (Master's or comparable degree, e.g., Diploma (Univ.) in Life Sciences, or Medical background
 For digital assets: hands-on experience of digital health asset project management and agile working methods

・Long term relevant experience in project management, preferably within the Pharmaceutical or Biotech industry
・Demonstrated understanding and application of broad portfolio of project management processes and tools; project management (PMP) certification desirable.
・Knowledge of pharmaceutical industry and experience in collaborating with related core and enabling functions. Relevant Therapeutic area expertise is required.

For digital:
・Knowledge and understanding of digital health asset development from ideation, MVP, to pilot pre-launch and in scaling and the running digital health assets and best practices
・Understanding of the digital health and medical device regulations landscape and experience with coordinating lean cross-functional teams in an agile and self-organizing work environment
・Critical thinking with the ability to influence, negotiate and manage conflicts at all levels to achieve team alignment, commitment to deliverables with positive team environment
・Strong communication skills, ability to present complex relationships in a concise and structured manner
・Proactive, strives to develop solutions and promote their acceptance. Experience in how to create and nurture a psychologically safe, try-and-learn work environment while keeping ambitious timelines
・Finding opportunities for standardization across assets based on interaction with peer program managers
・Act as task master, support asset teams in resolving issues quickly in line with AAI. Expert knowledge of agile principles and practices for software product development and delivery
【歓迎経験】
【免許・資格】
【勤務開始日】
応相談
学歴
大学院修士以上
雇用形態
正社員
試用期間
3ヶ月

勤務地
東京
勤務地(変更の範囲)

会社の定める事業所

転勤の有無
転勤なし
受動喫煙防止措置
屋内禁煙
勤務時間
フレックスタイム制
フルフレックス(コアタイムなし)
みなし労働時間/日:7時間45分
休憩時間:45分
<標準的な勤務時間帯>
8:45~17:20
勤務開始日
応相談
休日休暇
年間休日数:127
土日祝
年間有給休暇:入社直後4日 4日 ~ 13日
法定休暇:年次有給休暇、産前産後休暇
その他休暇:慶弔休暇・リフレッシュ休暇、整理休暇
年収・給与
年収  600万円~1300万円 経験により応相談
諸手当
・当社規定により経験に応じて優遇
・外勤手当、時間外手当、MR手当
昇給
年1回(4月)
賞与
賞与 固定賞与(夏・冬 各2.5ヶ月) および 業績賞与
採用人数
若干名
待遇・福利厚生
通勤手当:有
寮・社宅:有
福利厚生倶楽部、確定拠出年金(給与財源型/DC)と確定給付企業年金(リスク分担型/RSDB))、財形貯蓄、住宅取得補助手当制度(規定に準ずる)、医療費補助等
各種制度
健康保険:有
雇用保険:有
労災保険:有
厚生年金:有
退職金制度:有
選考プロセス
1)書類選考
2)一次面接
3)二次面接
4)最終面接

新着 外資製薬メーカー

プログラムマネージャー/ノンラインマネージャー /オンコロジー・免疫領域事業本部

  • 新着求人
  • 英語を活かす

※こちらに入力した項目が企業に直接届くことはございません。

この企業が募集している
他の求人

外資製薬メーカー

コマーシャルクオリティ…

仕事内容:
チーム員でこれらの業務を分担しています…
年収・給与:
600万円~
勤務地:
東京

外資製薬メーカー

品質管理 / スタッフ…

仕事内容:
【職務内容】 ・品質統括部の方針に基…
年収・給与:
500万円~
勤務地:
山形

外資製薬メーカー

EHS(シニアスタッフ)

仕事内容:
グループ各社(NBI/BIS/BIAH…
年収:
経験により応相談
勤務地:
東京

外資製薬メーカー

Manager, Ex…

仕事内容:
1. 積極的なアカデミア(大学、研究機…
年収:
経験により応相談
勤務地:
兵庫

外資製薬メーカー

工場デジタルトランスフ…

仕事内容:
・Conduct continuous…
年収:
経験により応相談
勤務地:
山形

外資製薬メーカー

工場プロセスマネジメン…

仕事内容:
1. 製造管理関連業務(GMPソフト)…
年収:
経験により応相談
勤務地:
山形

外資製薬メーカー

工場品質保証スタッフ …

仕事内容:
【職務内容】 ・製品出荷及び記録書類…
年収・給与:
500万円~
勤務地:
山形

外資製薬メーカー

Manager | n…

仕事内容:
・Key Job Accountabi…
年収・給与:
600万円~
勤務地:
東京

新着外資製薬メーカー

Financial c…

仕事内容:
・Supporting overall…
年収・給与:
600万円~
勤務地:
東京

外資製薬メーカー

FBA Manager…

仕事内容:
Accountabilities 1…
年収・給与:
600万円~
勤務地:
東京

外資製薬メーカー

Marketing G…

仕事内容:
Accountabilities * …
年収・給与:
600万円~
勤務地:
東京

外資製薬メーカー

Product Man…

仕事内容:
Ensure achievement …
年収・給与:
600万円~
勤務地:
在宅可、東京

※こちらに入力した項目が企業に直接届くことはございません。