医師転職・バイトは民間医局

兵庫県神戸市・内科・小児科の常勤医師求人（26-JZ316043）

お気に入り 問い合わせる
    • NEW
    • 常勤
    • 企業
    • 土・日・祝休み可
    • 当直なし
    • オンコールなし

    大手外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-JZ316043

    担当エージェントより

    募集形態：Senior Clinical Pharmacology Lead/ノンラインマネージャー or スタッフ/医薬開発本部臨床薬理部
    対象専門科目：内科、小児科、アレルギー科、免疫科
    勤務地
    兵庫県神戸市
    路線
    科目
    内科・小児科
    勤務内容
    メディカルドクター
    勤務内容詳細
    Basic purpose of the job
    Senior CPhL-Asia supports the clinical development in Asia of new drugs and further development of approved drugs with emphasis on the design and execution of the Clinical Pharmacology (CP)development strategy.
    CPhL-Asia is accountable and responsible for communicating with regulatory authorities on CP topics and for CP aspects of drug submission in Asia (e.g., submission summaries).
    CPhL-Asia may act as trial clinical Pharmacologist (TCP; see TCP job profile) for clinical studies in their own project or outside of their own projects.
    CPhL-Asia may serve as Clin Pharm representative within various teams in Asia (Japan/China) in support of early integration of Japan/China into global development program. Post PoCP, they may serve as CP and TMCP representative in various Asian teams until submission and launch. CPhL-Asia will also serve as main TMCP representatives in all PMO projects in Asia.

    Accountabilities
    Ensure timely delivery of state-of-the-art Clinical Pharmacology scientific concepts for decision making throughout clinical drug development and registration in Asia including all necessary processes and documentation.
    Ensures timely delivery of state-of-the-art Clinical Pharmacology strategy development and implementation.
    Senior CPhL-Asia is responsible for defining the CP strategy (for instance, defining the drug-drug interaction liability or formulation development strategy for modified release) of assigned project. CPhL-Asia is also responsible for refining the CP strategy in a timely manner as new data become available during drug development. As part of the strategy, CPhL-Asia may define CP aspects in a clin trial protocol and for an eventual submission and further phase IV activities.
    Senior CPhL-Asia contributes to the Clin Pharm section of official documents (e.g., Information Brochure (IB), label); CPhL-Asia engages with regulatory agencies on matters pertaining to CP during drug development and are responsible for supporti
    給与
    1,100万円～1,400万円（スキル・経験による）
    勤務日数
    月曜～金曜（配属先部門によりシフト勤務・フレックスタイム制の適用有り）
    日程/時間
    8:45～17:20 ※休憩時間：45分

    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
    年間休日131日（2025年度実績）、完全週休2日制（土日祝日）、年末年始、ゴールデンウイーク、お盆期間を中心に年3回程度の長期休日あり、初年度入社時有給休暇：10日　等
    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
    Minimum Education/Degree Requirements
    Master's degree (or equivalent) in Medicine, Pharmaceutics, CP or equivalent area of focus with preferably 5-6 years of relevant experience in CP in the pharmaceutical industry, regulatory agencies, or academia could be considered for this position.

    Doctoral degree (MD or PhD) in Medicine, Pharmaceutics or CP. Prior CP experience (around 2-3 years) in the pharmaceutical industry, regulatory agencies, or academia preferred.

    Required Capabilities (Skills, Experience, Competencies)
    Language skills: English: fluent (Read/Write/Speak).

    Mindful of local, global, internal, and external cultures to ensure that messages are received positively and effectively.

    Evidence of strong teamwork, also in global and remote context.

    Good interpersonal skills with the ability to interact effectively with people, internally and externally (e.g., CROs, experts, management).

    Ability to pro-actively identify issues and solutions and to interact with internal and external bodies on TMCP issues.

    Ability to lead and facilitate meetings.

    Ability to develop and deliver training related to TMCP topics required.

    Experience working in the matrix, act in matrix leadership.
    Very good knowledge in PK and PK/PD, Clinical Pharmacology, biopharmaceutics, clinical drug development and relevant regulatory guidelines. Good understanding of pharmacometric tools (modeling and simulation), their opportunities and limitations as well as basic understanding of statistical principles especially with respect to Clin Pharm trial data.

    この求人情報の詳細は
    お気軽にお問い合わせください。

    • 先生の個人情報は許可なく求人先にお伝えすることはありません。
    • 匿名にてお問い合わせ内容を確認いたします。
    お気に入り 問い合わせる

関連の求人

内科系 他科系 内科・一般内科 小児科 関西 大阪 企業 当直なし 土・日・祝休み可

今の検索条件で非公開求人の紹介を受ける

医師の求人のほとんどは非公開求人です。お探しの条件にあった非公開求人をご紹介します。

紹介を受ける