薬事
Development Regulatory Affairs Manager
薬事

Development Regulatory Affairs Manager
の転職・求人情報はすでに掲載終了しております。(掲載期間8月27日~10月21日)

※ 掲載時の募集要項はページ下部よりご確認いただけます。
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ミドルの転職では、各専門分野のコンサルタント6189が紹介する316755の転職情報を掲載しています。
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職種、勤務地、年収などを組み合わせて探すことができます。
掲載時の募集要項掲載期間:2024/08/27 ~ 2024/10/21)
薬事

Development Regulatory Affairs Manager

外資系企業 上場企業 大手企業 管理職・マネジャー マネジメント業務なし 新規事業 転勤なし 土日祝休み

募集要項

募集背景
新規雇用
仕事内容
Development Regulatory Affairs Manager, individual contributor role
Group Purpose:
Facilitate patient access to company products in Japan through executing the development and regulatory plans; providing strategic regulatory expertise for drug development; interfacing with agencies on regulators; aligning with key cross-functional partners; integrating into the company’s commercialization process, and continuously improving our processes and developing our talent.

Job Summary:
- Conducts regulatory activities for company products in Japan
- Support drug development or commercialization activities in Japan based on the regulatory and submission strategy by serving as Japan Regulatory Lead (JRL)
- Develop and maintains good relationship with Japanese Health Authorities to facilitate drug approvals.
- Provide regulatory guidance and supports various internal teams by involving Japan Development Team and Global Regulatory Team.
応募資格
必須
Knowledge And Skills
- Over 10 years experiences in pharmaceutical industry including at least 5 years experiences in regulatory affairs with experiences conducting PMDA consultations and CTN submission in Japan.
- Applies analytical skills to evaluate and interpret complex situations/problems using multiple sources of information.
- Independently develops solutions that are thorough, practical and consistent with functional objectives
- Ability to understand scientific/clinical information
- Organizational, communication and time management skills needed to manage multiple assignments and processes
- Communication skills in English
- Native level Japanese
- Computer skills
- Bachelors in scientific discipline
歓迎
Preferred
- More than 5 years experiences in development regulatory affairs working on oncology/hematology drugs.
- TOEIC score ≥780, desirable
- Advanced degree preferred.
募集年齢(年齢制限理由)
定年退職年齢の上限の為 (定年年齢を上限として募集するため)
雇用形態
正社員
勤務地
関東、関西
年収・給与
~ 1100万円ベース給与 + 15%変動賞与
選考プロセス
面接2回(通常な場合)
一回目:日本メンバー
二回目:グローバルダイレクト報告先

会社概要

社名
非公開
事業内容・会社の特長
One of the most innovative pharmaceutical companies that harnesses the best of biology and technology, use technology and human genetic data to push beyond what's known today to fight the world's toughest diseases, and make people's lives easier, fuller and longer.
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