Grupo Sanofi Argentina (Genzyme, Aventis and Pasteur) Pharmacovigilance Associate (South Cone) In charge of South Cone (Argentina, Uruguay and Paraguay) Pharmacovigilance Process included Individual Case Safety Report (ICRS) to Global/Local authorities, follow-up, RMP, Local Literature Review.Main activities and responsibilities1. Responsible for carrying out the Pharmacovigilance tasks concerning Sanofi-aventis, Sanofi Genzyme, Sanofi-Pasteur products within the Southern Cone (ARG, PRY, URY).2. Responsible for collecting, reporting and processing adverse events and security information reported by patients and health professionals both spontaneous and resulting from programs to support physicians and / or patients to local health authorities (ARG, URY, PRY).3. Perform and follow-up of risk management plans with medical affairs.4. Responsible for maintaining RMP local tracking5. Responsible for maintaining the PV Records and Documentation.6. Training to the members involved in the market-patient support program surveys and review of surveys, QC and reconciliations.7. Provide support in reviewing and maintaining the (auditable) PV regulatory documentation in accordance with GCP guidelines and ICH standards.8. Responsible for maintain the tracker related “Local Literature Review of Adverse Events” for ARG, URY, PRY.9. Responsible for Local Literarure Review for ARG, URY, PRY.10. Responsible for handling issues related to drug safety.11. Responsible for drafting procedures, manuals, work guides related to Pharmacovigilance for Southern Cone

Inmunoterapia en cáncer .Fundación Instituto Leloir. CABA, Argentina Sep-2015/Present Scientific Investigation. Department of Oncology. Collaboration with the Department of Cancerology for the study of immunotherapy in cancer in murine model to learn new skills in laboratory and to obtain a degree in master of Medical Molecular Biology, with the main objective of know and improve in the future the efficacy of antitumoral vaccine in skin cancer.Main activities and responsibilities1. Produce vaccines with dendritic cell for skin cancer to perform laboratory tests and study their efficacy in murine model.2. Preclinical investigation3. Use of some equipment: Microscopy, laminar air flow cabinet, Flow Cytometry4. Management of Cell culture for study cancer process.5. Scientific investigation related immunotherapy in cancer

Janssen de México S.A. de C.V., México, DF. Jan-2013/Jun-2014 Regional Pharmacovigilance Specialist (Latin American).In charge of Latin American Regional Pharmacovigilance Process, built a new process of Execution of Follow-up attempts, specific questionnaires of adverse events reports for drugs marketed by Janssen, with an improvement in the number of follow-ups from this new implementation, with 100% compliance and with the Regional compliance excellence award. Main activities and responsibilities 1. Execution of Follow-up attempts of adverse events reports in Latin America, these activities involved the communication with Pharmacovigilance Managers (Local SafetyOfficer, LSO) and also were an opportunity to keep a continuous improvement process. 2. Monthly Compliance for the whole Latin America, maintaining communication of all queries by the LSO. 3. Communication and Interaction with Call Center Supervisor and Call Center Agents in Mexico and Brazil for continuous training on issues related to pharmacovigilance. 4. Quality Review in local procedures relating to pharmacovigilance activities in Call Center of Mexico

Drug Safety and Epidemiology.Novartis Pharmaceuticals, México, DF. May-2008/Dec-2012 1.Pharmacovigilance Jr Associate.2. Pharmacovigilance and Medical Information Associate3. Scholarship holder of Pharmacovigilance and Medical Information.Managed of Medical Information and Pharmacovigilance Process accordance with local and global authorities, also support of other areas as Clinical Safety, Regulatory affairs, marketing programs.Main activities and responsibilities1. Handling, sending, processing and follow-up attempts of adverse events reports from any source according to global and local regulations.2. Contribution in the review of standard operating procedures accordance with local and global authorities.3. Management of good clinical practice, risk management plans, clinical trials and marketing programs.4. Active participation, support and management about requirements in marketing programs related to Pharmacovigilance.5. Responsible for the process, communication and delivery of international reports clinical safety studies to health authorities. 6. Visits to sites with clinical monitors to verify pharmacovigilance processes7. During my work in Medical Information were sent approximately 1,200 scientific articles within a year, generating interest and commitment in health issues with physicians.