Clinical Trial Associate H/F

Ipsen

Les Ulis

Purpose of the position
• Assists and provides support to the members of the clinical operations study team in administrative activities in order to facilitate the overall management of Company sponsored studies
• Executes tasks as assigned by the CPM related to the conduct of clinical studies, study budget forecasting and tracking
• Responsible for collecting, tracking and supports reporting of research related Transfer of Value (TOV) to enable compliance with Transparency reporting requirements (US and EU)
• Responsible for ensuring study documentation (including trial master files, study related contracts and financial level documentation) and study documentation is processed, maintained/archived in compliance with ICH-GCP, Company policy and procedures. Includes liaison with service providers in regards Ipsen e-TMF process and resolving issues related to missing documentation
• Performing QC checks on TMFs to ensure completeness and readiness for audit/inspection
• Contributes to... More Detail

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