Associate, CRA
募集要項
JoB No. | 435 |
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業種 | 製薬メーカー |
ポジション名 | Associate, CRA |
職種 | 臨床開発 |
業務内容 |
• Performs site selection for potential sites to evaluate their capabilities for conducting a clinical trial. Recommends sites to participate in clinical trial. • Performs Site Initiation Visit, ensures site personnel is fully trained on all trial related aspects. Performs continuous training for amendments and new site personnel as required. Retrains site personnel as appropriate. • Performs continuous monitoring activities (onsite and remote). Implements site management activities to ensure compliance with protocol, GCP, global and local regulations, global and local processes to secure data integrity and patient safety. • Performs Site Closeout activities per SOPs and applicable regulations to ensure that site is aware of any follow up activity and archiving requirements. • Collaborates with Clinical Study Manager and Medical Science Liaison to ensure recruitment plans and execute contingency plans, as needed. • Play a role in the global development of innovative drugs (antibody drug, tumor immunotherapy, regenerative medicine, etc.). |
勤務地 | 東京都 |
応募資格 |
Education: Degree in scientific or healthcare discipline. Languages: Experience/Professional requirement: Competencies: Skills & Knowledge: You’ll receive: (not mandatory)
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雇用形態 | 正社員 |
年収目安 |
年収400万~700万
残業代別 |
備考 | --- |
担当コンサルタント | 小川 善之 |
企業情報
企業名 | — |
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事業内容・会社の特徴 | — |
その他の求人情報
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