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求人ID : 1422942 更新日 : 2024年04月27日
Hybrid work - Competitive Salary

Senior Program Manager - Pharmaceuticals Company ~ 20M

採用企業 One of the world's largest pharmaceuticals company
勤務地 東京都 23区
雇用形態 契約
給与 1600万円 ~ 2000万円

ワークスタイル

リモートワーク・在宅勤務 服装カジュアル 副業OK 残業少なめ フレックスタイム制

募集要項

Planning:

  • Compile individual project plan to develop program roadmap
  • Maintain and update overall program roadmap
  • Identify projects issues / risks / interdependency across projects and monitor based on development
  • Update program team structure with relevant key stakeholders (where required)
  • Handle global touch points for global initiatives (where required)
  • Initiate way forward planning with prioritized business / system issues /constraint in capacity

 

Delivery:

  • Run weekly tracking cadence with Project Managers
  • Track and monitor progress of individual projects
  • Escalate risks and issues to relevant stakeholders with proposed resolutions/ actions
  • Provide updates to program key stakeholders regularly 
  • Conduct monthly Steering Committee (“SC”) meeting
  • Prepare for SC meeting agenda and decks
  • Coordinate program level meetings and document key actions and decisions
  • Facilitate meetings to achieve expected outcome
  • Follow up on key action items
  • Develop other key program documents, as required
  • Provide resolution/ intervention at project level (if required) to help remove barriers
  • Assist in budget tracking by  liaising with individual project managers to compile the cost incurred and share with finance team

 

応募必要条件

職務経験 10年以上
キャリアレベル 中途経験者レベル
英語レベル 流暢 (英語使用比率: 75%程度)
日本語レベル 流暢
最終学歴 大学卒: 学士号
現在のビザ 日本での就労許可が必要です

スキル・資格

• Act as central point of contact for vendor providing this service.
• Assist CPL with Interactions with CRO and site staff to adhere to study budgets.
• Requests accruals, and performs contract and invoice review.
• Participate in operation meetings with CRO, and cross-functional team members; document escalations and actions.
• Coordinate study team training in the investigator portal; monitor site/CRA user access and track compliance during the study.
• Coordinate with CPL and cross-functional team to assemble study documents as appendices for CSR at study close-out.
• Upon site closure, prepares subject files, inventories documents, reconciles document discrepancies, and organizes study files for electronic archive and off-site storage.
• SME for initiatives in conjunction with the CoE, as required to ensure consistent implementation

勤務地

  • 東京都 23区

労働条件

雇用形態 契約
給与 1600万円 ~ 2000万円
業種 医薬品

職種

  • ICTスペシャリスト(IT・Web・通信系) > プロジェクトマネージャー

会社概要

会社の種類 大手企業 (300名を超える従業員数) - 外資系企業
外国人の割合 外国人 半数