Aurélien Blondel

Clinical Project Leader @Alzprotect Sas

Région de Lille, FR

Coordinate exchanges regarding national or international clinical trials in relation with the internal team and the providers involved- Ensure close interaction with functional experts and key opinion leaders involved in the clinical study- Manage the electronic and paper archives of documents related to clinical research- Implement and follow up actions to respect recruitment deadlines and good clinical practices- Discuss and manage study plans, timelines and budget with selected CROs and external vendors from initial planning to final reporting phase- Participate in the drafting and review of documents related to clinical research (Protocols, ICFs, etc.)- Contribute to the selection of CROs and external providers to conduct and plan assigned clinical studies- Contribute to the implementation and follow-up of clinical trials: documentation, regulatory and budgetary aspects- Acquire and maintain specialized technical and regulatory knowledge related to clinical research activities

University of Montpellier

Master 2 (M2), Management des Opérations Cliniques

Lycée Jean Perrin

Baccalauréat Scientifique, Mention Très Bien, Spé Physique Chimie, Section Européenne Anglais

Faculté des Sciences Pharmaceutiques et Biologiques de Lille

Docteur en pharmacie