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東京都の臨床開発・薬事の求人193件応募資格・募集要項・仕事内容を見る
Clinical Scientist (Oncology)
- 給与
- 記載なし
- 勤務地
- 東京都
- 休日
- 記載なし
- 雇用形態
- 記載なし
どんな仕事かAIによる生成
The Clinical Scientist in Japan is responsible and accountable for clinical scientific outputs for assigned projects and studies, with accountability for approximately 2 - 4 projects (assets) at any one time. The role provides scientific leadership for Japan clinical development strategy, plans and studies, and works collaboratively with Japan and global teams to drive project success.
この求人に応募
応募資格
必須
- MD (Japan licence)
- Scientific, medical and regulatory knowledge including disease, treatment and guidelines.
- Strategic assessment and decision making skills for designing clinical development plans and clinical studies.
- Ability to interface with relevant scientific external stakeholders (e.g. regulators, EEs, CROs, investigators) to deliver clinical studies.
- Creative thinking skills for developing innovative business solutions.
- Solid understanding of clinical research and biostatistics principles to facilitate innovative and efficient clinical trial design with clear data-driven decision rules.
- Ability to use judgment, statistics, and visualization techniques to analyze and interpret moderately complex information.
- Ability to lead scientific interactions and respond confidently to complex questions using sound judgment.
- Knowledge about the importance of work undertaken in support of the medicine/vaccine vision and lifecycle management plan.
- Experience contributing to projects and working collaboratively with multiple stakeholders.
- Ability to research and use data from various sources to make robust fact-based decisions, employing diverse and critical thinking.
- High-level English and fluent Japanese communication skills.
募集要項最終確認 10/30
- 職種
- 臨床開発・薬事
- 雇用形態
- 記載なし
- 給与
- 記載なし
- 勤務地
- 東京都
- 働き方
- 記載なし
- 掲載日
- 2026/10/29 15:17（1日前）
- 最終確認
- 2026/10/30 00:32（今日）
仕事内容
Job Purpose
- The Clinical Scientist (CS) in Japan is responsible and accountable for clinical scientific outputs for assigned projects and studies in Japan.
- The CS will have accountability for approximately 2 - 4 projects (assets) at any one time and they will be required to work collaboratively alongside Japan Development, Japan Regulatory Affairs, Japan Medical and other J-MDT/VDT colleagues, as well as with global Medicines/Vaccines Development Team (MDT/VDT) and Clinical Sciences members to drive the ongoing success of the projects
Key Responsibilities
- Provide matrix leadership in Japan clinical team (Clinical Science, Clinical Operations, Medical Writing, Biostat, Data Management, etc.) to ensure integrated approach, robust planning, and execution oversight.
- Provide expert leadership and asset/disease expertise
- for Japan clinical development strategy and plan (e.g., clinical positioning, clinical development plan, clinical study design) to deliver differentiated medicine/vaccine of value for patients, stakeholders and markets in Japan.
- for Japan clinical study (e.g. Protocol, ICF, CTN, SAP) and clinical regulatory (e.g. CTD, briefing documents for consultation, and answers to queries from Regulatory authority) related documents.
- Serve as a co-decision maker (along with JMDL/JVDL/CDL) to resolve disputes among the Japan clinical team.
- Collaborate with central clinical team to create global/Japan clinical development strategy and plan that supports optimal medicine/vaccine development for Global as well as Japan.
- Represent the Japan clinical development of the project internally (e.g., central Clinical Science, functional leaders, senior managements, governance boards) and externally (e.g., MHLW/PMDA. EEs/HCPs, Patient Groups)
- Evidence Outputs: In terms of Japan analyses, interpret study data to create the scientific content of Clinical Study Report (CSR) and prepare the abstracts, posters and presentations for scientific meetings, congresses, external journal publications.
- Ensure quality & compliance oversight in Japan clinical development which align with R&D expectations, project needs, regulatory requirements including risk management, and escalate where required.
- Foster accountability culture: empower Japan clinical team members with clear ownership of tasks, support escalation when risks emerge, and celebrate delivery successes.
この求人は、グラクソ・スミスクライン株式会社の採用ページの内容をAIが読み取って整理したものです。応募の前に採用ページの原文を確かめてください。データの集め方企業サイト
同じ会社の求人8件
- Clinical Development Lead/CDL or Sr. Clinical Scientist/CS
- 薬事オペレーション部長
- Compliance Director – Business Partnering & Advisory
- Head of Vaccine / Infectious Disease Medical Affairs
- Principal Statistician
- Senior Manager, Business Development
職種と勤務地が似ている求人東京都の臨床開発・薬事 193件
- RA Manager
- Senior Regulatory Affairs Specialist (シニア薬事スペシャリスト )
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- 臨床開発モニター
- 薬事申請資料のQC、作成サポート業務
- CMC Regulatory Affairs Specialist
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応募はグラクソ・スミスクライン株式会社の採用ページで受け付けています。このページは採用ページの掲載内容をもとに構成しているため、最新の応募条件は募集元でご確認ください。
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