Fabiana Dutra Esquivel
São Paulo
Visão geral
13
13
years of professional experience
14
14
years of post-secondary education
Experiência profissional
Pharmacist - 24-hour Emergency Unit
AHBR - Brazilian Hospital Association
Várzea Paulista, SP
2024.12 - 2025.04
- Responsible for the organization, control, dispensing, and distribution of medications and medical supplies across hospital sectors, following technical and administrative procedures;
- Supervise stock levels in both physical inventory and management systems;
- Oversee preventive and corrective maintenance of pharmacy equipment and infrastructure;
- Manage and lead the pharmacy team, ensuring compliance with organizational and departmental regulations and effectively addressing operational challenges.
Clinical Trials Assistant in Drug Safety
IQVIA (sponsored by ROCHE)
São Paulo, São Paulo
2016.04 - 2018.04
- Processed clinical trial safety data, reviewed inconsistencies, and liaised with research centers to resolve discrepancies;
- Ensured the translation and entry of applicable safety data into the Serious Adverse Event (SAE) database;
- Participated in the review of existing standard operating procedures (SOPs);
- Collaborated with the Project Physician and/or Medical Officer as required.
Pharmacovigilance Analyst
Hypera Pharma
São Paulo, São Paulo
2014.02 - 2016.01
- Evaluated, classified, and analyzed adverse drug events according to WHO guidelines on severity and causality;
- Used MedDRA terminology to complete CIOMS forms;
- Conducted proactive case investigations with patients and healthcare professionals;
- Submitted adverse event reports to Brazilian regulatory authorities and business partners;
- Processed case reports in the Organex Safety Information Solution (SIS);
- Created case narratives for healthcare professional reports to notify the Health Surveillance Center (CVS).
Pharmacovigilance Analyst
Takeda Pharmaceuticals
São Paulo, São Paulo
2011.11 - 2012.04
- Conducted pharmacovigilance activities for all registered and marketed Takeda products;
- Performed individual case safety reviews, collected, monitored, researched, and assessed safety data from healthcare professionals and patients;
- Submitted reports to health authorities, partners, and stakeholders;
- Conducted signal detection and assessment, benefit-risk evaluation, and safety risk management;
- Ensured compliance with US, EU, and international pharmacovigilance regulations, including GCP, GVP, and GMP;
- Prepared periodic safety update reports for local health authorities.
Formação acadêmica
PhD - Parasitology, Genetics, and Epidemiology
Institute of Biomedical Sciences / University of São Paulo
2018.07 - 2024.12
Exchange student - Public Health and Biochemistry
College of Charleston
2013.01 - 2013.12
Bachelor’s Degree - Pharmacy and Biochemistry
School of Pharmaceutical Sciences / University of São Paulo
2009.03 - 2016.04
Habilidades e competências
- Strong communication skills within teams
- Willingness to work collaboratively
- Excellent interpersonal skills for teamwork
- Commitment to continuous learning and professional development
Idiomas
English
Avançado
C1
Espanhol
Intermediário
B2
Linha do tempo
Pharmacist - 24-hour Emergency Unit
AHBR - Brazilian Hospital Association
2024.12 - 2025.04
PhD - Parasitology, Genetics, and Epidemiology
Institute of Biomedical Sciences / University of São Paulo
2018.07 - 2024.12
Clinical Trials Assistant in Drug Safety
IQVIA (sponsored by ROCHE)
2016.04 - 2018.04
Pharmacovigilance Analyst
Hypera Pharma
2014.02 - 2016.01
Exchange student - Public Health and Biochemistry
College of Charleston
2013.01 - 2013.12
Pharmacovigilance Analyst
Takeda Pharmaceuticals
2011.11 - 2012.04
Bachelor’s Degree - Pharmacy and Biochemistry
School of Pharmaceutical Sciences / University of São Paulo
2009.03 - 2016.04