Are you passionate about improving patient outcomes? Do you have experience in medical affairs and a desire to make a difference in the healthcare industry? We are looking for a Medical Advisor to join our dedicated
開発部門では国内外で実施する臨床試験の企画・管理・モニタリングなど様々な業務を行っており,チームで企画からモニタリング業務まで担当します。 企業情報 * 外資系製薬会社 * イノベーション:研究開発への投資を通じて、新しい医薬品や治療法の開発に取り組んでおり、疾患の治療と予防に貢献しています。 * 将来の医療ニーズに対応するために多岐にわたる製品パイプラインを保有しています。 職務内容 * 治験実施計画書、同意説明文書及び症例報告書の作成(補助) * モニタリング計画書等、各種手順書の作成 * モニタリングおよび施設対応の実施責任者として、モニターを指揮して治験を実施 * モニタリング報告書・必須文書・症例報告書等の確認 * 担当試験に係わるチーム内(モニター)教育 理想の人材 * 臨床開発のモニタリング経験 * リーダーシップ、コミュニケーション、プレゼンテーションのスキル 条件・待遇 * 休日:日曜日、祝日、年末年始、会社指定休日 * 賞与:あり * 加入保険:雇用保険、労災保険、厚生年金、健康保険 Page Group Japan is acting
* Takes accountability and serves as the first line of contact at the study level. 企業情報 * Top 3 Pharmaceutical Company * Rich pipeline with nice promotion space 職務内容 * Takes accountability and serves as the
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Responsible for executing the following basic MSL tasks under the guidance of his/her superior and the support of a senior MSL. • Responsible for building trust relationship with Key Individuals (KIs) in their therapeutic area and
Responsible for executing the following basic MSL tasks under the guidance of his/her superior and the support of a senior MSL. • Responsible for building trust relationship with Key Individuals (KIs) in their therapeutic area and
Responsible for executing the following basic MSL tasks under the guidance of his/her superior and the support of a senior MSL. • Responsible for building trust relationship with Key Individuals (KIs) in their therapeutic area and
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
Do you enjoy a role in management? Are you interested in helping to shape a new solution in Japan About our Team Elsevier Health applies innovation, facilitates insights, and helps drive more informed decision-making for our
* Manage timely product approvals for target indications in Japan * Align with global strategies and Japanese healthcare requirements * Collaborate across departments for regulatory compliance * Develop and update Japanese clinical development plans * Handle submissions