Browse our jobs and apply for your next role.
The right candidate is just a few clicks away.
PageGroup changes lives for people through creating opportunity to reach potential.
If you have any questions, we’re here to help.
- CSS (Company-led research)- IIS (Doctor-led research)- Collaborative study- Including oversight of external CRO
現在、治験薬管理のお仕事をされている方で、大手製薬企業(外資)にて、幅広い治験薬管理の業務に携わりたい方にお勧めの求人です。
臨床試験実施計画書の作成、モニタリング計画書の作成モニタリング業務(医療機関への臨床試験モニタリング、調査報告書の作成等)進捗管理(モニタリング報告書、進捗状況報告書の作成等)
Maintains effective collaborative partnership with all stakeholders, ensuring aligned and synergistic approach to site's experience with interactions.
企業治験、医師主導治験、臨床研究におけるプロジェクトマネジメント、モニター業務、臨床研究管理全般
Responsible for the supervision of assigned direct reports within Clinical Operations, FSP and/ or Sub-CRO Services Staff
グローバルに展開する大手製薬企業で、日本臨床開発において臨床開発戦略、臨床試験の設計、実施、解釈を推進し、臨床試験における医学的説明責任と監視の主要な役割を担っていただきます。
Responsible for designing, validating, and implementing EDC clinical trial setups, along with creating data cleaning solutions.Opportunity to contribute to cutting-edge drug development research with collaborations with various multinational pharmaceutical businesses.
Create Job alert to receive 治験 jobs via email the minute they become available
Submit your CV to register with us and we will contact you if a suitable role becomes available.