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. |
---|---|
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 - その他 |
業種 | 製薬メーカー |
勤務地 |
アジア
日本
東京都
|
仕事内容 |
Be part of one of the top global pharma companies in the industry. Take lead in new drug application submission to obtain regulatory approval. Description * Take lead in regulatory strategy/development to obtain product approval * Provide regulatory expertise in collaboration with global stakeholders to develop product plan * Submit documents to obtain PMDA approval * Update any regulatory changes when necessary Profile * University degree in scientific environment or related areas * High fluency in English and Japanese (non-native speakers will not be selected) * RA experience in the pharmaceutical industry * Ability to communicate with global stakeholders as well as local health authorities (PMDA) Job Offer * Competitive salaries and benefits * Great work life balance * International working environment * Hybrid working style * Amazing career progression in RA * Work with industry leaders who are solving various unmet medical needs To apply online please click the 'Apply' button below. For a confidential discussion about this role please contact Saki Kanematsu at +81 3 6832 8904. |
企業について (社風など) |
* One of the largest global pharmaceutical companies in the industry * Rich development pipeline with constant development for new products * Specializing in oncology, rare disease, infectious disease, respiratory, etc. * Global culture with extensive communication with stakeholders * Hybrid working style |
英語能力 | ビジネス会話 (TOEIC 735-860) |
日本語能力 | ネイティヴレベル |
年収 | 日本・円 1000万円 〜 1500万円 |