Sophie KeuferLe Gall Email & Phone Number | Head of clinical department (4 years): -Contribute to the clinical development plan for several compound (Major Depression Disorder, Alzheimer disease, Neuropathic pain...) -Write clinical protocol, write clinical part of regulatory's documents, Manage team International Clinical Project Manager (5 years): Accountable for Phase II to Phase IV studies - Scientific part: write clinical protocol and develop study documents (monitoring guide, medical review guide, SAP....) -Operational part: Set-up and follow-up trials (select/train/follow external vendors, follow recruitment, follow budget and timelines, organise international investigator's meetings...) Monitoring Project Manager (5 years): Accountable for set-up and coordination of clinical studies - Phase I, II, and III (Neurology – Psychiatry – Cardiology – Ophthalmology) - Manage CRAs team (10 CRAs) - Perform feasibility study– preliminary visits – Sites’ selection - Prepare and lead local investigators’ meetings/ Monitors’ meetings

Sophie KeuferLe Gall

Head of clinical department (4 years): -Contribute to the clinical development plan for several com...
France

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Sophie KeuferLe Gall’s Email legals@roche.com

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Sophie KeuferLe Gall’s Location France

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Global Studies Leader

2020-09-01 00:00:00 - Present

Head Of Clinical Department

2011-01-01 00:00:00 - 2015-12-01 00:00:00

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Sophie KeuferLe Gall is a Head of clinical department (4 years): -Contribute to the clinical development plan for several compound (Major Depression Disorder, Alzheimer disease, Neuropathic pain...) -Write clinical protocol, write clinical part of regulatory's documents, Manage team International Clinical Project Manager (5 years): Accountable for Phase II to Phase IV studies - Scientific part: write clinical protocol and develop study documents (monitoring guide, medical review guide, SAP....) -Operational part: Set-up and follow-up trials (select/train/follow external vendors, follow recruitment, follow budget and timelines, organise international investigator's meetings...) Monitoring Project Manager (5 years): Accountable for set-up and coordination of clinical studies - Phase I, II, and III (Neurology – Psychiatry – Cardiology – Ophthalmology) - Manage CRAs team (10 CRAs) - Perform feasibility study– preliminary visits – Sites’ selection - Prepare and lead local investigators’ meetings/ Monitors’ meetings