Thiago Sabino

Experience

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  Hospital Beneficencia Portuguesa de São Paulo

  May 2013 - Dec 2013

  Clinical Pharmacist

  • Monitoring of clinical parameters and monitoring of low therapeutic index drugs, nephrotoxic drugs, immunosuppressants and antibiotics, in addition to trigger drugs. • Pharmacovigilance activities.

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  Hospital Sírio-Libanês

  Jan 2014 - Feb 2018

  Clinical Pharmacist

  • Responsible for the specialties of Cardiology, Gastroenterology and Urology, evaluating prescriptions and planning pharmaceutical interventions. • Monitoring of clinical parameters and monitoring of low therapeutic index drugs, nephrotoxic drugs, immunosuppressants and antibiotics, in addition to trigger drugs. • Pharmacovigilance activities. • Management of a team with more than 20 assistants and technicians, support with logistical planning for the acquisition of medicines.• Experience with Swisslog and Pyxis technology. Show less

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  Universidade de São Paulo

  Mar 2018 - Dec 2021

  • Assisting the Clinical Research Coordinator in clinical study management activities. Ensures the integrity of clinical data and study are conducted in compliance with approved protocol, GCP, applicable regulations and SOPs.• Responsible for recruitment, engagement and retention; development of the annual plan of study actions and events; Application of strategies for follow-up and retention study volunteers.• Informed consent application.• Volunteer organization schedule, preparation of visit files, doubts and requests related to health care. Show less

  • Research Coordinator

    Jan 2021 - Dec 2021

  • Clinical Research Assistant

    Mar 2018 - Dec 2020
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  Hospital Sírio-Libanês

  May 2023 - Oct 2023

  Pharmacist

  • Team management with more than 20 assistants and technicians • Interaction and interventions with healthcare team regardless of medical prescription;• Support to logistical planning for the acquisition of medications; • Provision of pharmaceutical assistance; • Experience with Swisslog and Pyxis technology;• Development of inclusion and diversity projects for new employees;

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  P+F Products + Features GmbH

  Mar 2024 - now

  Clinical Affairs

  • Responsible for manage daily activities involving the acquisition, updating, and upkeep of clinical trial data.• Provision assistance in clinical research operations and the evaluation process.• Collaborate on analyzing clinical data pertinent to product life cycles.• Contribute to project management tasks and facilitate communication between internal teams and external stakeholders, notably Contract Research Organizations (CROs).• Provide expertise and operational assistance for post-market surveillance and risk management procedures concerning products. Show less