Lead and supervise the logistics operations and project management team for the clinical trials in Latin America. Supervise and coordinate the logistic operations team to comply with quality standard, local regulations as well as with GMP, GCP and GDP. Client relationship management for all the projects ongoing.

Statistical consultant at FICConsultor Metodología y Estadística de la Investigación, asesoramiento técnico metodológico de los proyectos científicos de la Fundación en todas sus etapas: planeamiento, diseño del estudio, diseño de muestreo y de instrumentos de recolección de datos, análisis de resultados, redacción y publicación de informes y/o artículos científicos.

Lead health information and Statistics office at the Ministry of Health of Buenos Aires city, with the objective of providing timely and quality information to strengthen decision-making. Organize and develop the data governance strategy across the public health organizations. Provide methodological support for the impact evaluation. Develop the KPI's to follow and monitoring different projects and programs within the Ministry and other Government Areas. Lead the health data science projects… Show more Lead health information and Statistics office at the Ministry of Health of Buenos Aires city, with the objective of providing timely and quality information to strengthen decision-making. Organize and develop the data governance strategy across the public health organizations. Provide methodological support for the impact evaluation. Develop the KPI's to follow and monitoring different projects and programs within the Ministry and other Government Areas. Lead the health data science projects. Coordinate information management and maintenance of area databases. Make management reports and publications. Strengthen the continuous team training. Show less

Lead and coordinate the clinical research studies in Latin America. Act as the main nexus among the sponsor and the Investigators. Build the metrics at Latin American level for the studies ongoing in the region. Report on progress of the project to all stakeholders and present reports defining project progress. Coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices.

Build the dashboard with the relevant metrics for the studies ongoing and maintain consistency in the study data across the LA region. Coordinate the study start-up activities, site recruitment and Budget Process for the clinical research studies performed in LA. Support study process to ensure adherence to protocol, SOPs, GCP/ICH Guidelines, applicable regulatory requirements in Latin America. Communicate and interact with site staff, project team, and the sponsor.

Provide support to the Regional Clinical Operations Team in the Medical Business Planning and implementation of clinical studies within the intercontinental region.Lead/coordinate business processes and contribute on key projects to improve information management and analysis for the Region.Direct Report: Intercontinental Business Operations Team Leader

Collaborate on Overseeing the progress of a clinical trial, and ensure that it is conducted, recorded and reported in accordance with the protocol, standard operating procedures (SOP´s), GCP/ICH, and the applicable regulatory requirements.

To measure the productivity and performance of the Latin America affiliate and generate valuable information at diferent levels (Affiliate, Region, trial, etc) through data available in different System used within Lilly.

Metrics and Reporting to Product Managers + Marketing Director. / Support to Sales Force with Training and reporting.