東京都新宿区・内科の常勤医師求人(25-JQ306044)

    • 常勤
    • 企業
    • 土・日・祝休み可

    大手外資系製薬メーカーでの就業です

    掲載更新日 : 2025年08月06日   案件番号 : 25-JQ306044

    担当エージェントより

    募集形態:Medical Advisor
    対象専門科目:内科(※免疫疾患、オンコロジー、代謝疾患、循環器疾患)
    勤務地:東京都新宿区
    勤務地
    東京都新宿区
    路線
    科目
    内科
    勤務内容
    メディカルドクター
    勤務内容詳細
    Medical Advisors provide medical and scientific expertise and guidance to investigators and CSU (Clinical Study Unit staff performing clinical trials within a CSU cluster to ensure patient safety and scientific integrity of the protocol which ensures the reliability of information provided to agencies at submission. They are therapeutically aligned medical experts in the country/region for the studies/projects they are responsible for. They provide appropriate medical and scientific feedback to Local CSU operations teams as well as global R&D Medical Operations, i.e., Clinical Research Director (CRD), Global Feasibility Lead (GFL), TA early planning leads, global project team, pharmacovigilance, and regulatory affairs. They ensure the medical and scientific collaboration with medical functions in the respective Business Units in the countries of their responsibility and with investigators, trialists, medical experts, and Key Opinion Leaders (KOLs) in the country, region, or global level.

    Provide medical/scientific value across a continuum of both external and internal stakeholders: e.g., Key external experts and other healthcare professionals within assigned therapy area or assigned programs, (potential) investigators, professional societies, and patient organizations.
    Review and resolve local medical issues / questions that arise during the entire course of the study and that arise from local regulatory authorities – if necessary, transferring issues to global teams.
    Proactively seek and collect the medical voice of the external experts, potential investigators and KOLs to facilitate the conduct of clinical trials. Through appropriate scientific exchange and scientific engagement with external stakeholders, secure advice that informs and assists internal strategic functions in the development of compounds.
    Act as the local medical expert to bring early input into study design and operational aspects.
    →備考に続く
    給与
    年収1,100万円~(目安の金額になります)
    ※経験・スキルによります。
    勤務日数
    週5日(月~金曜日)
    日程/時間
    9:00~17:15(実働時間7時間15分) フレックスタイム制あり ※休憩時間:60分
    オンコール
    休暇・研究日
    完全週休2日制、国民の祝祭日、年末年始、公民権行使・公務休暇、有給休暇(勤務年数に応じて付与最高20日/年)、その他慶弔休暇など
    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
    Provides timely medical training to local Monitoring Team, including training to CSU staff on protocols, therapeutic area, disease, products, medical environment, medical and/or scientific training to new hires.
    Provides medical and scientific advises to key internal stakeholders developing proposals: this may include, but is not limited to, reviewing the protocol for scientific/regulatory soundness and feasibility, providing medical/scientific insights on target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.
    Exchange information between R&D and other departments within the affiliate and contribute to Medical Department Team meetings related to the therapeutic area to ensure objectives of these meetings are met.
    Local scientific knowledge and lobbying allowing capture of country specific information on competitive intelligence and validation of global hypothesis from the Clinical Development Plan or assessment of Extended Synopsis (ES)/protocol contents.
    Liaise with local Medical Leads within Sanofi Global Business Units in his /her country(ies) to manage investigators and compounds.
    Support local/regional Investigator Meetings regarding medical content and interaction with investigators in collaboration with CRD.
    Ensure accuracy of translation of medical terms related to study documents when translated into the local language, including ICF, patient materials, wherever appropriate.
    Contribution to protocol optimization and standard of care assessment as a part of Pressure Test to position the study in the ecosystem and drive local strategy.
    Patient Network Engagement at local / regional level, being the link to Patient Informed Development & Health Value Translation Team.
    Collaborate with TA Lead providing impactful and relevant local information to support the Global Strategy per TA including information to support diverse study population.


    【必須条件】
    ・医師免許
    ・3~5年以上の臨床経験(※免疫疾患、オンコロジー、代謝疾患、循環器疾患)
    ・ICH、GCP、現地規制に関する知識
    ・ビジネスレベルの英語力

    【歓迎スキル】
    ・博士号

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