Responsable de projet clinique
Updated: April 13, 2024 08:22 AM GMT
NOVADIP Biosciences S.A.
Mont-Saint-GuibertYour Responsibilities
• You proactively manage assigned clinical trial timeline, budget and milestone achievement and are accountable for ensuring that all project deliverables meet Novadip’s expectations and standards.
• You coordinate and manage all operational aspects of clinical trial activities from study start-up (ie. conduct of the Trial Kick-off meeting, site selection and supporting CROs selection) to close-out activities
• You are familiar with strict deadlines to meet project timelines, with the ability to modify work schedule when needed.
• You coordinate & provide clinical input and/or develop study-related materials such as:
– Provide input/write/review clinical study documents and Plans (ie. Protocols, Clinical Monitoring Plan and all ad- hoc requested forms)
– Coordinate and perform site selection and IRB/EC submissions up to site initiation and activation
• You serve as the primary key contact person for study CROs (DM, safety/pharmacovigilance, statistics…... More Detail
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