大阪府・内科・外科の常勤医師求人(26-JZ316041)

    • NEW
    • 常勤
    • 企業
    • 土・日・祝休み可
    • 当直なし
    • オンコールなし

    大手内資系製薬メーカーでの就業です。

    掲載更新日 : 2026年10月06日   案件番号 : 26-JZ316041

    担当エージェントより

    募集形態:Associate Medical Director, Oncology Clinical Sciences, R&D, Osaka
    対象専門科目:内科、外科※抗がん剤治療の経験要
    勤務地
    大阪府
    路線
    科目
    内科・外科
    勤務内容
    メディカルドクター
    勤務内容詳細
    Job Description
    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.
    ACCOUNTABILITIES:
    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 develo
    給与
    1,500万円~2,000万円(スキル・経験による)
    勤務日数
    月曜~金曜
    日程/時間
    9:00~17:30 ※休憩時間:規定による

    夜診:なし
    早番:なし
    遅番:なし
    当直
    なし
    オンコール
    なし
    休暇・研究日
    土曜日、日曜日、祝日、メーデー、年末年始休暇など(年間約123日)、年次有給休暇、特別有給休暇、病気休暇、家族支援休暇、産前産後休暇、育児休暇、家族介護休暇
    勤務開始時期
    応相談
    医療機関情報
    医療機関形態:企業

    屋内の受動喫煙対策:あり(禁煙)
    備考
    Education & Competencies
    Education/Experience

    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.
    JNDA/NDA/MAA/Submission experience preferred
    Experience with and demonstrated ability to lead and manage highly trained medical, scientific and technical professionals preferred
    Skills

    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
    Knowledge

    Therapeutic area knowledge relevant to mechanisms of action of compounds in remit
    Regional/global Regulatory requirements
    GCP/ICH
    Emerging research in designated therapeutic area

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