• 企業プロフィール

• CRO（医薬品開発業務受託機関）事業

非臨床試験、臨床試験、開発計画、薬事コンサルティング事業を行っています。

世界の製薬メーカーをクライアントに持ち、プリファード契約もいただいています。開発・研究拠点を世界各地に持つCROで、医薬品開発事業の総合的なパートナーとして、開発計画から治験関連サービス、医薬品の上市のサポートに至るまで、幅広い専門的なサービスを提供しています。
Fortreaは以下のような価値を世界で提供しています。

• 勤務地

• 当社についてもっと知りたい方へ

• To assist CRAs with preparation for site visits, e.g. running reports, QC of files (checking for missing documents), resolving action items from previous visits.
• Perform Case Report Form review, query generation and resolution against established data review guidelines, under direct supervision on the Company or client data management systems, as assigned by management.
• To assist with the coordination of study visits and shipment of drug and laboratory samples.
• To manage sites to ensure subjects are complying with protocol requirements, study visits, and timelines.
• To liaise with the project team and others to distribute and track clinical trial supplies, e.g. Case Report Forms, study medication, lab kits, ensuring that sites have sufficient supplies to continue recruitment.
• To assist in submissions and notifications to Ethics Committees and Regulatory Authorities as applicable.

• Bachelor’s degree or above, or registered nurse or certified clinical technologist

• Business level English; TOEIC score above 740 during the last 1 year or equivalent