Work
Experiences

• 2023-2024

• HEALTHCARE ADVISOR

• HICKEY'S PHARMACY
• • Overall improvement in patient safety and healthcare understanding
  • Management, monitoring, and dispensing of prescriptions while providing expert supportive recommendations
  • Working in synergy with pharmacists and technicians, ensuring more than 200 high-grade processes per day according to SOPs
  • Inventory management and monitoring
  • Teamwork process optimization

• 2021-2023

• CLINICAL RESEARCH COORDINATOR

• BUTANTAN INSTITUTE

• Highlight: Managed Coronavac clinical trials in the field of immunology and vaccines, known as 'Project S', involving approximately 27,000 participants.

  • Assurance of workflows and safety standards according to the study protocol and ICH GCP
  • Trial Master Files management, maintaining and updating essential documentation
  • Compilation and submission of documents to ethics committees and regulatory authorities
  • Prompt conduction of more than 150 SAEs and SUSARs reports/monitoring activities
  • Serving as the primary contact for communication between investigators, sponsors, CROs, and other stakeholders.
  • Training, supervision, and enhancement of knowledge/skills for the research team
  • Data management
  • Tracking and managing budgets and timelines
  • Development and management of e-CRFs

• 2021-2021

• CLINICAL RESEARCH HEAD PHARMACIST

• CLINICAL RESEARCH CENTRE - S (CENTRO DE PESQUISA CLÍNICA - S)

• Highlight: Pharmaceutical operations supervisor and helped establish the Serrana Clinical Research Center in 2021.

  • IP inventory management, randomization, blinding, preparation, and dispensing
  • Track and document the receipt, distribution, and return of IPs
  • Working closely with investigators and monitors to design and implement study protocols
  • Ensuring study completion and participant safety and well-being

• 2021-2021

• CLINICAL RESEARCH ASSISTANT

• BUTANTAN INSTITUTE
• • Data collection and entry in e-CRFs
  • Organizing and updating trial-related documents, including consent forms, case report forms, and regulatory binders
  • Managing multiple studies, varying from 3k to 30k participants, including monitoring and ongoing communication
  • Monitoring and follow-up on SAEs
  • Conducting trial data analysis on a weekly basis, resulting in extremely accurate CRFs and maintaining outcome integrity

• 2017-2020

• SPECIALIST IN CLINICAL AND HOSPITAL PHARMACY

• Hospital Sírio-Libanês
• EQF level 8
• • Main high-level hospital in Latin America
  • Theoretical and practical training in clinical pharmacy and pharmacovigilance
  • Active methodological approach
  • Multisectoral approach aimed at involving different hospital units (including inpatient wards, emergency care, surgical center, and intensive care unit)