Ervelyne Carpentier

Clinical Lead @Iqvia France

Paris, FR

Responsabilities: • Manage the clinical operational aspects of a clinical trial to achieve the “rightsubject” and the “right data”.• Drive the clinical team (clinical study team, CRAs, CTAs) to reach project overallobjectives and milestones.• Accountable for the clinical delivery (recruitment, site management, dataintegrity, quality…) in accordance with Protocol, ICH-GCP and SOPs.• Key sponsor’s point of contact for clinical operational aspects.• Oversee the compliance of study systems: eTMF, eCRF, IWRS, internal systems.• Creation and maintenance of study plans, guidance, training materials,monitoring tools…• Involvement in preparation of audits/inspection and CAPA creation.• Oversee the compliance of study systems: eTMF, eCRF, IWRS, internal systems• Forecast the clinical activities for financial perspective.

Sup Santé

Attaché Recherche Clinique

University of Lille 1 Sciences and Technology

Master 1, Neurosciences et Physiologie Intégrée

University of Lille 1 Sciences and Technology

Licence, Biologie cellulaire et physiologie