María Arribas Gonzalez

Tasks: Process spontaneous and clinical trial adverse events reports, Data entry in the Global Safety database, International tracking, submit spontaneous an clinical trial individual case safety reports to the local Health Authorities, PSUR submission to Health Authorities

Tasks:, databases management, searching literature, review and develop of promotional and training materials, support and monitoring of epidemiological studies, publications and scientific materials, studies poster elaboration, coordination of national projects, attendance to meeting and conferences, working relationship whit Opinion Leaders, medical support for Marketing and Sales Force.

Main subjects: Drug discovery and pharmaceutical development, Drug research and development, Clinical trials management, Pharmacoepidemiology and Pharmacovigilance, Registration and Institutional Relations, Pharmaceutical Marketing, Pharmacoeconomics.