求人検索
この求人の 取扱い会社 |
マイケル・ペイジ・インターナショナル・ジャパン株式会社/Michael Page International Japan K.K. |
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企業名 | 会社名非公開 |
職種 |
メディカル/医薬/バイオ/素材/食品 - 臨床開発系
|
業種 | 製薬メーカー |
勤務地 |
アジア
日本
東京都
|
仕事内容 |
This pivotal role combines the excitement of crafting innovative clinical development strategies tailored to specific indications/products, ensuring their safety and efficacy for swift global registration, while also offering the opportunity to shape regulatory strategies and contribute vital medical insights to the prestigious Common Technical Document (CTD) Description 1 Drive high-quality clinical documents: Provide medical/scientific input for study protocols, reports, and publications. 2 Oversee medical monitoring and risk management: Guide trial teams and manage scientific risks. 3 Propose clinical strategies and liaise with stakeholders: Develop Japan-specific plans and collaborate with key stakeholders for successful registration. Profile * A Doctor of Medicine (MD) degree is required. * Prior experience in the pharmaceutical industry is essential. * Excellent command of English, coupled with native-level fluency in Japanese, is a must. Job Offer In this role, you'll have the exciting chance to create innovative clinical development strategies, ensure product safety and efficacy for global registration, shape regulatory approaches, contribute to the Common Technical Document (CTD), all while enjoying the flexibility of a highly hybrid workstyle. Page Group Japan is acting as an Employment Agency in relation to this vacancy. |
企業について (社風など) |
A prominent player in the pharmaceutical sector, this organization is globally acknowledged for its groundbreaking contributions, notably in the realm of immuno-oncology. |
英語能力 | ビジネス会話 (TOEIC 735-860) |
日本語能力 | 流暢(日本語能力試験1級又はN1) |
年収 | 日本・円 1600万円 〜 2000万円 |