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[Innovative Medicine] Project Lead, Regulatory Medical Writing, Japan Document Management Group, IB Translation Office/Publication Owner Office
年収：800万 ～ 1300万
採用企業案件
ヤンセンファーマ株式会社
-
- 会社規模501-5000人
- 医薬品メーカー
| 部署・役職名 | [Innovative Medicine] Project Lead, Regulatory Medical Writing, Japan Document Management Group, IB Translation Office/Publication Owner Office |
|---|---|
| 職種 | |
| 業種 | |
| 勤務地 | |
| 仕事内容 |
■Description At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. ■Job Description: As a core responsibility, manage the daily progress of projects for translation office (Protocol, IB) and Publication Owner. Additionally, own the transformation of the IB translation process from the traditional outsourcing model to an efficient process that applies the latest technology, such as AI translation. ■Key Responsibilities: Responsible for leading activities in the Translation Office and Publication Owner Office across all projects. Manages CRO throughout the project and gives instruction to FLEX staff for greater productivity. Perform proofreading after AI translation to ensure the draft quality meets PJ team review standards. Lead verification and operation of translation memory assets for the AI translation Be proactive in finding opportunities for greater efficiency and take the lead in finding and implementing flexible solutions. Can lead cross-functional or broader initiatives for process and business improvement. Strengthen team members and lead them to cultivate their development. |
| 応募資格 |
【必須（MUST）】 ■Education:A MS or other advanced degree with a minimum of 8 years of relevant pharmaceutical/scientific experience. A BS with a minimum of 10 years of relevant pharmaceutical/scientific experience. Experience and Skills: ■Required: A solid understanding of drug development is required. Strong project management skills are required. A PMP certification is highly desirable. Have interest and passion for groundbreaking technologies such as AI. Experience in working in cross-functional teams and supporting or leading large projects is required. Willing to build processes from a new point of view without being tied to existing processes. Understands J&J's CREDO based culture and has the willingness to grow while not only delivering results but also influencing those around them. 【歓迎（WANT）】 Have experience in clinical trial result publication and an understanding of the related processes.Proficient Japanese speaking/writing skills. Proficient business English conversation skills. Sophisticated IT skills. |
| 受動喫煙対策 | その他 「就業場所が屋外である」、「就業場所によって対策内容が異なる」、「対策内容は採用時までに通知する」 などの場合がその他となります。面接時に詳しい内容をご確認ください |
| 更新日 | 2026/03/18 |
| 求人番号 | 7822215 |
採用企業情報
- ヤンセンファーマ株式会社
-
- 会社規模501-5000人
- 医薬品メーカー
-
会社概要
私たちヤンセンファーマは、世界最大級のトータル・ヘルスケア・カンパニー、
ジョンソン・エンド・ジョンソン（J＆J）グループの製薬会社として、いまだ
満たされていない医療ニーズに迅速に応え、最先端の医薬品を一刻も早く患者
さんの手元に届けることができるよう取り組んでいます。
私たちは、世界57ケ国200社以上に及ぶJ＆Jグループを貫く経営理念「我が信条
（Our Credo）」を志とし、さらに、46年間に84品目もの新薬を開発したヤンセ
ン・ファーマスーティカ社の創業者、ポール・ヤンセン博士の妥協なき開発精
神を継承し、J＆Jグループの優れた新薬の導入はもちろん、医療現場への適切
かつ最新の医療情報の提供、さらには、患者さんのＱＯＬ（クオリティ・オブ・
ライフ）の向上を目指した支援活動などをおこなっています。
転職・求人情報の詳細をご覧になる場合は会員登録（無料）が必要です