Clinical Trial Assistant US
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About The Position
The position involves supporting clinical project management and monitoring of clinical studies. This includes liaising with monitors, CROs, drug vendors, central laboratories, and other vendors for study-related tasks. The individual will be an active member of the study team and will take responsibility for service provider oversight according to Ipsen procedures. Responsibilities also include monitoring, verifying, and archiving the Trial Master File (TMF) in accordance with Ipsen SOPs, ensuring quality and completeness for audits and inspections. Additionally, the role requires follow-up and review of financial documents in collaboration with Ipsen GCPM, including creating and updating financial information within Ipsen financial systems and assisting in budget forecasting and quarterly reviews.
