- グローバル基準の臨床試験に携わり、専門性を継続的に高められる環境
- ワークライフバランスと働きやすい制度が整った業界大手CRO
企業情報
国内外で臨床試験を幅広く支援している大手CROで、グローバルスタンダードに基づいた開発体制と質の高いプロジェクト運営で知られています。教育制度も充実しており、CRAが長期的にキャリアを形成できる専門性の高い環境を整えています。
職務内容
- 治験実施施設および担当医の選定・評価
- スケジュール管理や契約関連資料の確認、医療機関向け説明の実施
- 症例進捗管理、症例報告書(CRF)の収集・点検
- 治験薬の配送状況・管理状況の確認および回収
- モニタリング訪問および報告書の作成
- 治験終了時の手続きや必要書類の最終確認
- 若手CRAへの教育・サポート
理想の人材
- 3年以上のCRAのご経験がある方
条件・待遇
- 各種社会保険
- リモート勤務制度
- フレックスタイム制度
- 産前産後、育児サポート
- 勤務地:東京または大阪
Contact: Saki Nagao
Quote job ref: JN
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