JOBID:286871750366
Clinical Affairs Specialist / Clinical Site Operation (In‑house CRA)
アボットメディカルジャパン合同会社
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CRA・臨床開発モニター
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医療機器メーカー/医療関連サービス
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東京都
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600万円~900万円
募集要項
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- 職種
- CRA・臨床開発モニター
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- 業種
- 医療機器メーカー/医療関連サービス
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- 職務内容
- 【Primary Function】
This role is responsible for managing study documentation and operational progress using Clinical Trial Management System, while maintaining the highest quality standards in clinical study execution. The position oversees documentation and study management support across clinical studies, including clinical investigations, post‑marketing surveillance, and clinical research, ensuring that all clinical study data comply with applicable regulations and SOPs.
Leveraging prior CRA experience, this role as a Clinical Site Operation (In‑house CRA) provides the opportunity to oversee clinical studies from a broader perspective and to support both operational and quality aspects of study execution. Additionally, the role collaborates with APAC and global partners to drive continuous process improvements across the organization.
We seek individuals who can maintain the highest level of quality in clinical studies while proactively addressing new challenges and contributing to innovation across the organization. This position is ideal for those who aspire to pursue various career paths in the future, including People Manager and Project Manager roles.
【Major Responsibilities】
○ CTMS Management : Ensure compliance with clinical protocol and applicable regulatory requirements such as GCP, ISO14155 or GPSP through appropriate management, review, and maintenance of site-level TMF documentation in accordance with Work Instructions.
○ Study Management Supports: Maintain study progress in the CTMS. In partnership with Abbott assigned field staff and in-house personnel, coordinate and support site activation and site close-out activities for clinical studies, ensuring completion, accuracy, and compliance of all required documentation, processes, and study materials.
○ Study Document Development and Maintenance: Develop and update study specific documents in collaboration with internal/external personnel/parties.
○ Inventory Management for Clinical Trials: Manage clinical trial inventory in accordance with applicable regulations and internal procedures, including vendor management (e.g., courier and logistics providers), development of study
-specific Inventory Management Plan, and coordination of shipment and return instructions for investigational devices.
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- 勤務地
- 東京都
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- 給与
- 600万円~900万円
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- 給与(詳細)
- 経験・スキルをもとに優遇
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- 応募資格
- ○CRA経験 2年以上
○ビジネスレベルの英語力
○ Degree in science/health-related field (e.g., Biology, Nursing, Biomedical or Veterinary Sciences).
>2 Years of experiene in Field Clinical Research Associate, ensuring compliance with J-GCP, Ethical Guidelines for Medical Reserch Involving Human Subjectsm, and/or the Clinical Trial Act.
○ Fluent in English and Japanese (speaking, writing and reading).
○ Proven expertise in Microsoft Office Suite.
○ Working knowledge of medical terminology.
○ Excellent written and verbal communication skills, including negotiation and relationship management.
○ Strong problem-solving, organizational, analytical and critical thinking skills.
○ Full knowledge and understanding of GCP.
○ Detail oriented and good problem-solving ability.
○ Ability to interact with senior internal and external personnel on significant matters, often requiring coordination between organizations.
会社情報
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- 会社名
- アボットメディカルジャパン合同会社
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- 本社所在地
- 〒105-7115 東京都港区東新橋1-5-2 汐留シティセンター
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- 資本金
- 25億200万円
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- 従業員数
- 連結約2,300名
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- 企業の特徴
- アメリカ・イリノイ州に本社を持つAbbott Laboratoriesは1888年に創業され、世界100カ国以上で事業を展開するグローバルヘルスケア企業です。
日本においては、治療機器、臨床検査、糖尿病ケア、栄養製品の4つの事業領域で製品とサービスを展開しています。
同社の強みは、世界規模の研究開発力と、それを日本の医療ニーズに合わせて展開する柔軟性にあります。
グローバルで確立された技術と品質を、日本国内の医療現場に適した形で提供できる体制が整っています。
また、患者中心のアプローチを重視し、医師・医療従事者との連携のもと、QOLの向上につながる製品開発に力を入れています。
予防から診断、治療、健康維持に至るまで、人生のあらゆる段階で人々の健康を支えるトータルソリューションを提供していることが最大の特徴です。
転職相談
医療機器業界における転職やキャリア設計、
求人などまずはカジュアルにご相談を
承っております。