Responsable de projet clinique

Updated: March 23, 2024 09:42 PM GMT

Full-time Job in Mont-Saint-Guibert, Wallonia

NOVADIP Biosciences S.A.

Mont-Saint-Guibert

Your 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... More Detail