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東京都の臨床開発・薬事の求人136件応募資格・募集要項・仕事内容を見る
Medical Lead, Biopharma
- 給与
- 記載なし
- 勤務地
- 東京都中央区
- 休日
- 完全週休２日制（土曜・日曜）
- 雇用形態
- 正社員
どんな仕事かAIによる生成
The Global Medical Lead, Biopharma and Ophthalmology Development, will lead the clinical development of one or more biopharmaceutical research programs at any stage from pre-clinical to approval, especially gene and ribonucleic acid (RNA) therapy. The role oversees clinical trials, develops clinical development plans, leads development teams, and contributes to regulatory submissions and clinical trial data analysis.
この求人に応募
応募資格
必須
- Doctor of Medicine (M.D.), or equivalent degree from an accredited medical educational institution
- Board certification (active or prior) in a relevant specialty, such as neurology, neurosurgery, or physical medicine and rehabilitation
- Unrestricted medical licensure in one or more jurisdictions
- 3 or more years of clinical practice experience
- 3 or more years of biopharmaceutical industry experience
- Proficiency with written, visual, and oral communication of medical knowledge
- Proficiency with Microsoft Office (Word, Excel, Power Point, One Note, Outlook, Share Point, and Teams)
- Proficiency with accessing, reading, and interpreting primary medical and scientific literature
- Proficiency with work in a cross-functional, matrixed, work environment
- Proficiency with people of diverse cultural backgrounds and geographic origins
- Working knowledge of biostatistics
- Fluent in written and verbal English
- Valid identification and up-to-date vaccination history to facilitate domestic and international travel
- Significant and demonstrable working-knowledge of regulatory procedures and guidelines in all regions (global scope)
- Proven record in clinical study design, monitoring and execution and results analysis
- Has demonstrated knowledge of designing, implementing, and conducting clinical studies, to produce both timely and high-quality data.
- Proven record of working on teams and in a matrix environment.
- Proven ability to get results in a matrix management environment.
歓迎
- Training in a relevant subspecialty, such as vascular neurology, neurocritical care, or stereotactic and functional neurosurgery.
- Clinical research experience as a site investigator or sub-investigator on a clinical trial
- Ph.D., M.S., post-doctoral laboratory research experience, or equivalent scientific training
- At least one scientific or clinical publication
- At least one scientific or clinical presentation at a regional or national meeting
- Phase 1 clinical trial experience
- Experience working in gene therapy, RNA therapy, or stroke drug development
- U.S. F.D.A. Pre-IND, IND, and BLA submission experience
- E.U. E.M.A. CTA and MAA submission experience
- Proficiency with Medidata Rave and Veeva Vault
- Working knowledge of artificial intelligence system use (e.g., Microsoft CoPilot)
- Experience in development and implementation of global clinical trials for the registration and support of new molecular entities worldwide
募集要項最終確認 10/11
- 職種
- 臨床開発・薬事
- 雇用形態
- Employment Class: Permanent期間の定めなし試用期間原則なし
- 役職
- Medical Lead
- 給与
- 記載なし
- 給与の詳細
- ①当人の経歴・技術・技能等を考慮して決定②中長期インセンティブ報酬:株式報酬有り有り
- 手当
- 住宅手当通勤手当
- 勤務地
- 東京都中央区 アステラス製薬 日本橋事業所 本社
- 転勤
- 会社の定める事業場および自宅
- 働き方
- At Astellas we recognize the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home.Hybrid work from certain locations may be permitted in accordance with Astellas’ Responsible Flexibility Guidelines.
- 勤務時間
- 管理監督者 8:45～17:45（月～木）、8:45～16:00（金）
- 休日・休暇
- 完全週休２日制（土曜・日曜）祝日5月1日夏季年末年始年次有給休暇育児休業制度介護休業制度 等
- 福利厚生
- 共済会制度社宅制度持株会制度財形貯蓄制度 等
- 社会保険
- 雇用保険、労災保険、厚生年金、健康保険
- 業務の変更の範囲
- 会社内での全ての業務
- 就業場所の変更の範囲
- 会社の定める事業場および自宅
- 経験年数
- 3年以上
- 学歴
- 大学院修了以上
- 選考の流れ
- 書類選考 → 1次面接 → 最終面接※変更の可能性もございますので、予めご了承下さい。
- 掲載日
- 2026/10/11 09:00（2日前）
- 最終確認
- 2026/10/11 19:20（2日前）
仕事内容
募集の背景 / Purpose & Scope
- The Global Medical Lead (GML), Biopharma and Ophthalmology Development (BOD), will lead the clinical development of one or more biopharmaceutical research programs at any stage from pre-clinical to approval, especially gene and ribonucleic acid (RNA) therapy. The GML will join a team of physician scientists reporting to the Global Medical Portfolio Lead, Biopharma and support the mission of BOD to create VALUE for patients.
職務の内容 / Essential Job Responsibilities
- oversee ongoing clinical trials to ensure the safety and well-being of clinical trial participants.
- design the overall clinical development plan for their assigned programs.
- draft protocols and supporting documents required to conduct individual clinical trials.
- direct a team of one or more development scientists and/or physicians in pursuit of program goals.
- contribute to global regulatory submissions.
- analyse, interpret, and disseminate clinical trial data internally and externally.
- prepare written and visual materials required for internal decision-making.
- collaborate with personnel from operations, regulatory, biostatistics, project management etc.
- educate and advise internal stakeholders as a subject matter expert in clinical medicine.
- engage with external stakeholders including physicians, regulators, advocates, patients, and caregivers.
- evaluate the clinical development feasibility of new business opportunities.
- 会社内での全ての業務
就業環境に関する要件 / Specific Physical or Environmental Requirements
- At Astellas we recognize the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home. We believe this will optimize the most productive work environment for all employees to succeed and deliver. Hybrid work from certain locations may be permitted in accordance with Astellas’ Responsible Flexibility Guidelines.
- This position requires approximately 25% travel, including domestic and international travel
この求人は、アステラス製薬株式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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募集元の採用ページから応募できます
応募はアステラス製薬株式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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応募資格の語から探す
- 医師66
- Microsoft Office983
- Word5,020
- Excel7,902
- PowerPoint4,446
- Microsoft Outlook308
- SharePoint154
- Microsoft Teams883
- 英語12,462
- データ分析5,721
- 臨床開発・薬事299
- AI5,495
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