Experience

• 

  Cemec pesquisa clínica

  Aug 2014 - Feb 2016

  Clinical trial intern

  - Pharmacovigilance reports submission (CIOMS);- Participation at the recruitment process of potential participants for clinical studies; - Patient care according to clinical protocol procedures and biological samples processing; - Clinical studies of cardiology, vascular, endocrinology, nephrology, gynecology.

• 

  Faculdade de medicina da usp

  Oct 2015 - Nov 2016

  Undergraduate student researcher -hiv

  - Study of viral evolution in HIV-1 infected patients treated with therapeutic vaccine;- Video conferencing and meetings to discuss scientific projects and articles;- Responsible for performing DNA extraction and quantification techniques, nested-PCR, electrophoresis, purification of PCR products, Gene Sequencing Reaction, basic analysis of gene sequences by software.

• 

  Hospital alemão oswaldo cruz

  Feb 2017 - Dec 2017

  Clinical trial intern

  - Responsible for regulatory processes such as submission, notification and pharmacovigilance reports to IEC and CONEP; - Monitoring of medical chart, recording and correction of CRFs; - Preparation of visits templates and documents to export biological samples;- Contact with monitors, sponsors, follow-up initiation and close out visits;- Clinica Studies of oncology, vascular, nephrology and respiratory diseases.

• 

  Instituto do câncer do estado de são paulo - icesp

  Sept 2018 - May 2019

  Clinical trial assistant - data entry

  - Data entry – Responsible for record all clinical data and queries resolution in CRFs; - Verification of source document quality and internal monitoring;- Clinical studies in oncology.

• 

  Iqvia

  Jun 2019 - now

  • Clinical Research Associate II (FSP Roche) | IQVIA

    Feb 2022 - now

  • Clinical Research Associate I (FSP Roche)

    Aug 2020 - Feb 2022

  • Clinical Trial Assistant (FSP Roche)

    Jun 2019 - Jul 2020