Found Description
Become a Clinical Trial Associate with ICON plc, leading healthcare intelligence in a remote role. Drive clinical development by executing oversight responsibilities, ensuring inspection readiness, and collaborating with teams.
In this remote position at ICON plc, you will be responsible for maintaining study inspection tools and coordinating TMF/Master File quality control. You will collaborate closely with CROs and the extended study team to ensure compliance with study oversight plans and deliverables, as well as support key startup activities for studies.
Key Responsibilities:
• Execute sponsor oversight responsibilities and maintain inspection readiness
• Coordinate TMF/Master File quality control activities
• Customize expected document lists with CRO collaboration
• Support compliance and quality deliverables
• Manage internal study trackers and collaboration systems
Requirements:
• Bachelor’s degree in medical or biological science
• Knowledge of c...
In this remote position at ICON plc, you will be responsible for maintaining study inspection tools and coordinating TMF/Master File quality control. You will collaborate closely with CROs and the extended study team to ensure compliance with study oversight plans and deliverables, as well as support key startup activities for studies.
Key Responsibilities:
• Execute sponsor oversight responsibilities and maintain inspection readiness
• Coordinate TMF/Master File quality control activities
• Customize expected document lists with CRO collaboration
• Support compliance and quality deliverables
• Manage internal study trackers and collaboration systems
Requirements:
• Bachelor’s degree in medical or biological science
• Knowledge of c...
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