Currently working in phase III multicentric clinical trials for dyslipidemia, including studies open label, blind and double blind for Hypercholesterolemia and Lipoprotein (A).• Provide overall support to the medical team in phase III studies.• Filling out CRFs with patients medical information and their follow up, including query resolution (Database Systems: iMedidata, Inform, Veeva,).• Ressuply investigational product via dispensing the IWRS (Systems: Suvoda, Cenduit, Signant Health).• Accompany patients during the visits.• Direct contact with sponsors and CROs to resolve pending issues (MSD, Novartis, Amgen, Eli Lilly);• Coordinate and manage the shipment of international biological samples.• Scheduling patients visits.• Maintain the Investigator Site File (ISF) and research participant binders.• Recruit potential research participants.• Support the medical team in patient screening.• Monitor hospitalizations to report SAEs and endpoints.• Ensure proper storage to drugs and accountability of all drugs.• Perfom drug accountability for patient adherence.• Coordinate necessary supplies for the study (lab kits, medication, patient's diary).• Participation in Monitoring Visits and SIVs.

I worked as an intern involving phases II, III and IV of clinical trials in rare diseases, focusing on Fabry Disease; Pompe Disease; Gaucher Disease; Mucopolysaccharidosis (MPS I) and Hunter Syndrome (MPS II), ensuring protocol compliance and Good Clinical Practice.• Provide overall support to the coordinators.• Maintained the Investigator Site File (ISF) and research partcipant binders.• Receveid training on regulatory processes (IRB, Brazil plataform).• Scheduled procedures/exams according to the study window.• Trained in CRF data entry (supervised).• Training about feasibility, site initiation visit and site qualification visit.• Collecting data for phase IV studies and updating it on eCRF.• Resolved queries for phase IV studies.

I worked on an epidemiological project about the impact of vaccination against COVID-19 in rate lethality on patients with cancer treated at institution, correlating with the immunization in São Paulo. Supervised by Dr. Gisele Fernandes and Dr. Maria Paula Curado.• Electronic database search.• Data collection in medical records.• Database structuring.• Statistical Analysys (IBM SPSS; Stata15).• Presentation of seminars in scientific events.• Scientific reports and writing.• Public data gathering.