Vanessa Fernandes

- Technical support to CRAs ensuring the efficient fulfillment of clinical trials’ deadlines; - Preparation of all documentation for the investigational sites initiation; - Preparation of documentation for submissions to Administration Boards; - Physical and Electronic archive of relevant regulatory documentation for clinical trials’ conduction; - Management of payments to suppliers ; - Organization of national and international Investigators’ meetings; - Local Key User of International eTMF of Boehringer Ingelheim; - Periodic Completeness and Quality Checks of eTMF; - Local Key User of international Boehringer Ingelheim Clinical Trial Portal (eISF); - Provide Training on Clinical Trial Portal to clinical operations team and site team; - Update of Clinical Trial Management System;