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大阪府の臨床開発・薬事の求人60件応募資格・募集要項・仕事内容を見る
Associate Medical Director, Oncology Clinical Sciences, R&D
- 給与
- 記載なし
- 勤務地
- 大阪府
- 休日
- 年間休日123日
- 雇用形態
- 正社員
- ハイブリッド勤務
- 在宅勤務あり
- フレックス
- 年間休日120日以上
- 賞与あり
- 退職金あり
どんな仕事かAIによる生成
Leads global clinical development strategy and multidisciplinary clinical teams for assigned oncology pipeline compounds. Oversees development plans and protocols, study execution and interpretation, medical monitoring, and interactions with regulatory authorities and key opinion leaders.
この求人に応募
応募資格
必須
- MD or internationally recognized equivalent plus 3 years of clinical research experience within the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical experience within academia (or a combination of afore mentioned).
- Previous experience successfully leading a clinical development team/matrix team with responsibility for studies.
- Superior communication, strategic, interpersonal and negotiating skills
- Ability to proactively predict issues and solve problems
- Ability to drive decision-making within a multi-disciplinary, multi-regional, matrix teams
- Diplomacy and positive influencing abilities across multinational business cultures
- Therapeutic area knowledge relevant to mechanisms of action of compounds in remit
- Regional/global Regulatory requirements
- GCP/ICH
- Emerging research in designated therapeutic area
歓迎
- JNDA/NDA/MAA/Submission experience preferred
- Experience with and demonstrated ability to lead and manage highly trained medical, scientific and technical professionals preferred
募集要項最終確認 10/15
- 職種
- 臨床開発・薬事
- 雇用形態
- Worker Type EmployeeWorker Sub-Type RegularTime Type Full time
- 役職
- Associate Medical Director
- 給与
- 記載なし
- 給与の詳細
- Salary Increase: Annually, Bonus Payment: Twice a year
- 手当
- CommutationHousingOvertime Work
- 勤務地
- Osaka, Japan
- 転勤
- It is possible the department and workplace may change at the company’s discretion.
- 働き方
- Flexible Work Styles: Flextime, Telework
- 勤務時間
- Working Hours: Headquarters (Osaka/ Tokyo) 9:00-17:30
- 年間休日
- 123日
- 休日・休暇
- SaturdaysSundaysNational HolidaysMay DayYear-End HolidaysAnnual Paid LeaveSpecial Paid LeaveSick LeaveFamily Support LeaveMaternity LeaveChildcare LeaveFamily Nursing Leave
- 福利厚生
- Flexible Work Styles: Flextime, TeleworkBenefits: Social Insurance, Retirement and Corporate Pension, Employee Stock Ownership Program, etc.
- 社会保険
- Benefits: Social Insurance, Retirement and Corporate Pension, Employee Stock Ownership Program, etc.
- 業務の変更の範囲
- It is possible the job scope may change at the company’s discretion.
- 就業場所の変更の範囲
- It is possible the department and workplace may change at the company’s discretion.
- 経験年数
- 3年以上
- 学歴
- 大学院修了以上
- 掲載日
- 2026/10/11 11:08（5日前）
- 最終確認
- 2026/10/15 09:15（1日前）
仕事内容
OBJECTIVES/PURPOSE:
- Leads and drives strategy for the overall global clinical development taking into consideration the medical, scientific, regulatory and commercial issues for multiple pipeline compounds.
- Applies clinical/medical decision making to clinical development issues.
- Influences senior leadership decision-making by setting strategic direction as well as by advocating for, designing, aligning, piloting and establishing new development processes that require cross-functional collaboration within Takeda R&D.
- Success or failure directly translates to the ability to meet its corporate goals and for Takeda to have future commercial products.
- Lead a multidisciplinary team (ie GCL). In this context knowledge, expertise needs to go beyond clinical and disease-area expertise to include broader areas of drug development (working knowledge of CMC, Commercial, etc.).
- Oversees medical monitor or clinical programs.
- Will have leadership of multidisciplinary clinical sub teams.
Clinical Development team participation and leadership
- Leads the Global Development Team (US, EU, Japan) managing both the US/EU Development Team and the Japan Development team for assigned compounds. In some cases may lead the US/EU Development Team but more likely will oversee the clinical scientist responsible for leading this team. Emphasis will be on insuring that the development teams are proactively identifying contingencies, potential risks and strategies to address future obstacles.
- Directs Development Team strategy and deliverables overseeing the Development Strategy, Clinical Development Plan and Clinical Protocols. Recommends scope, complexity and size, which influence the budget of all aspects of a program. Provides continual critical evaluation of the development strategy to maintain a state-of-the-art development plan that is competitive and consistent with the latest regulatory requirements, proactive identification of challenges, and development of contingency plans to meet them.
- Responsible for high impact local decisions: monitoring and interpreting data from ongoing internal and external studies, assessing the medical and scientific implications and making recommendations that impact local development such as “go/no go” decisions or modification of development plans or study designs that may have a significant impact on timelines or product labeling. Plans clinical development strategies in context of medical/clinical significance considering how a given product will fit in with current treatments, standard of care, and unmet medical need. A significant error in judgment may result in loss of approvability and/or commercial viability of a product.
Synopsis / Protocol Development, Study Execution, & Study Interpretation
- Drives all Clinical Science department activities relating to the preparation / approval of Synopses, Protocols and the conduct of clinical studies. Serves as an advisor to the clinical scientists involved in these activities, and be accountable to senior company management for the successful completion of underlying objectives. For the assigned compounds, accountable for the successful completion of projects undertaken - and for pro-active contingency planning / interventions necessary to ensure achievement of related goals.
- Interprets data from an overall scientific standpoint as well as within the context of the medical significance to individual patients.
Trial Medical Monitoring
- Oversees medical monitoring activities, assessing issues related to protocol conduct and/or individual subject safety. Assesses overall safety information for studies and compounds in conjunction with Pharmacovigilance.
External Interactions
- Directs activities involved in interactions with regulatory authorities/agencies and clinical development and key opinion leaders relevant to assigned compounds. Provides leadership and serves as an advisor to the other clinical scientists engaged in these activities and, in the context of these responsibilities, will be accountable to senior leadership for the successful completion of related objectives.
Leadership, Task Force Participation, Upper Management Accountability
- Interacts directly with research division based on pertinent clinical and development expertise and with US/EU to provide knowledge/understanding of market environment in line with status as R&D scientific content matter expert for assigned compounds. Represents clinical science on high impact/priority task forces across the organization or external to the company. Leads R&D internal teams and global cross-functional teams.
- Hires, manages, mentors, motivates, empowers, develops and retains staff to support assigned activities. Conducts performance reviews and drive goal setting and development planning.
この求人は、武田薬品工業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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職種と勤務地が似ている求人大阪府の臨床開発・薬事 60件
- メディカルアフェアーズ 専門マネージャー
- Manager, Safety Management, Patient Safety ＆ Pharmacovigilance Japan
- eCTD編纂業務（英語ファシリテーションあり）
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募集元の採用ページから応募できます
応募は武田薬品工業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
- 臨床開発・薬事307
この職種で探す
- 臨床開発・薬事307
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- 医療職3,274
- 薬剤師949
- 児童指導員・生活支援員634
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働き方・年収で探す
- 年収400万以上37,934
- 在宅勤務あり21,305
- フレックス23,856
- 年間休日120日以上35,417
- 賞与あり36,044