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東京都の臨床開発・薬事の求人248件応募資格・募集要項・仕事内容を見る
Senior Scientist or Scientific Advisor, Oncology
- 給与
- 記載なし
- 勤務地
- 東京都
- 休日
- 記載なし
- 雇用形態
- 正社員
どんな仕事かAIによる生成
This position serves as the affiliate’s medical and scientific expert for assigned products and therapeutic areas, with a primary focus on real-world evidence generation. It supports medical strategy, evidence development and study execution, IIS activities, and scientific exchange with external stakeholders.
この求人に応募
応募資格
必須
- Knowledge of medical science and regulations – Required
- Excellent oral and written English communication skill – Required
- Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols – Required
- Bachelor or Master of Science – Required
歓迎
- Experience of job in pharmaceutical company over 3 years – Desirable
- Ph.D. – Desirable
募集要項最終確認 11/13
- 職種
- 臨床開発・薬事
- 雇用形態
- Full-time
- 役職
- Senior Scientist
- 給与
- 記載なし
- 勤務地
- Minato City, Tokyo
- 働き方
- 記載なし
- 学歴
- 大学卒業以上
- 掲載日
- 2026/11/13 18:42(1日前)
- 最終確認
- 2026/11/13 18:42(1日前)
仕事内容
Summary of Job Description:
- Reporting to the Medical Affairs Manager, this position serves as the affiliate’s medical and scientific expert for the assigned product(s) and therapeutic areas, with a primary focus on real-world evidence generation activities. The role is responsible for partnering with the TA/MSL medical team, Evidence Solutions Group, and other internal and external stakeholders to develop evidence concepts and protocols, support study execution, and strengthen the scientific foundation of the assigned therapeutic areas. It also supports the identification, review, and management of Investigator-Initiated Studies (IIS), while engaging with external stakeholders to exchange scientific insights and advance evidence generation strategies.
Major Responsibilities:
- Contribute to and support the medical strategy for the assigned therapeutic area, with emphasis on real-world evidence generation.
- Collaborate with the TA/MSL medical team, Evidence Solutions Group, and other relevant internal and external stakeholders to develop evidence concepts, study proposals, protocols, and IIS-related activities.
- Support the planning, review, and management of real-world evidence generation activities and IIS in alignment with internal standards and applicable procedures.
- Establish and maintain professional relationships with external stakeholders, including academic experts and other relevant partners, to support evidence generation and scientific exchange.
- Review and synthesize relevant scientific literature, congress data, and external insights to identify evidence gaps, scientific trends, and opportunities relevant to the therapeutic area.
- Serve as a scientific resource for the assigned therapeutic areas, including responding to medical and scientific information requests and contributing to core medical materials and dossiers.
- Ensure all activities are conducted in compliance with applicable laws, regulations, industry codes, and AbbVie standards and policies.
この求人は、アッヴィ合同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
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応募はアッヴィ合同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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- 英語18,771
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