António Da Silva Pinto

Experience

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  Miranda e Ribeiro, Lda - Billabong Ericeira

  Sept 2006 - Sept 2007

  Salesman / Vendedor - Atendimento ao Publico

  Work in the same company in the summer months between 2008 and 2011.

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  Centro Hospitalar de Torres Vedras - Serviço de Medicina Transfusional

  Nov 2011 - Nov 2011

  Internship / Estagiário

  Voluntary internship at the Imuno-Hematology Laboratory

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  Centro Hospitalar Torres Vedras

  Jan 2012 - Jun 2013

  Biomedical Laboratory Scientist / Técnico de Análises Clinicas

  Work Areas:- Hematology, Clinical Chemistry, Imunology, Microbiology;- Analitical Results Validation- Collecting, screening and processing of all types of biological products

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  Miranda & Ribeiro , Lda - Billabong Ericeira

  Jul 2013 - Jul 2014

  Salesman / Vendedor - Atendimento ao Publico

  - Management Support- Sales

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  Psilexis - Centro Clínico

  Sept 2013 - Jun 2014

  Biomedical Laboratory Scientist / Técnico de Análises clinicas

  Collecting Biological Products

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  Clinica CUF Torres Vedras

  Jul 2014 - Jul 2014

  Biomedical Laboratory Scientist / Tecnico de Análises Clínicas

  Clinical Pathology Laboratory - Germano de Sousa

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  CHO- Centro Hospitalar do Oeste - Unidade Caldas da Rainha

  Aug 2014 - Jun 2015

  Biomedical Laboratory Scientist / Tecnico Análises Clinicas

  - Hematology, Clinical Chemistry, Imunology, Microbiology- Tecnical Responsible for the Hematology Section- Analitical Results Validation- Collecting, screening and processing of all types of biological products

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  Eurotrials

  Jul 2015 - Dec 2017

  All CRA related activities including:- Preparation, Performing, Follow-up on Qualification, Initiation, Monitoring and Close-Out Visits;- Investigator Site File/Pharmacy File Review;- Source Data Verification;- IP Accountability, Return and Destruction;- Communication with all trial related staff (Investigators, Sponsor's project team, Pharmacists, Laboratory Staff, External Vendors, others);- Trial Supplies Management;- Site Selection Activities;- Protocol Compliance Verification;- Protocol Deviation Identification, Reporting and Follow-up;- Submission Essential Documents Collection;- IP Release Package Documents Collection;- Audit Preparation, Support and Follow-up including CAPA Implementation;- Business Development;- Database Lock Support Activities;- Query Follow-up and Resolution;- Annual Progress Report Preparation;Therapeutic Areas: Immunoalergology, Gastroenterology, Pediatric Pain; Show less - Preparation and collection of essential documents in accordance with the client's Standard Of Procedures (SOP's) and local regulatory applicable requirements from EC and RA's;- Preparation of IP Release Package for IMP shipment to site;- Investigator Site File and Pharmacy File preparation and shipment to site;- Follow-up on SAE outcomes with the sites;- Trial Master File preparation, maintenance and shipment to Central File; - Communication with all trial related staff (Investigators, Sponsor's project team, Pharmacists, Laboratory Staff, External Vendors, others);- Support in Newsletter's elaboration and distribution to site ;- CRA support in Preparation and Follow-up of Initiation and Monitoring Visits;- Preparation and Follow-up on Audits;- CRA back up activities;- Site Payments; Therapeutic Areas:Pediatric Pain, Gastroenterology, Ophtalmology, Cardiology, Rare Diseases, Rheumatology. Show less

  • Clinical Research Associate I

    Apr 2016 - Dec 2017

  • Clinical Trials Assistant / Clinical Monitoring Associate

    Jul 2015 - Dec 2016
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  CTI Clinical Trial and Consulting Services

  Dec 2017 - now

  CTI is an innovative, international drug and device development organization that delivers a full spectrum of clinical trial and consulting services from bench to commercialization

  • Clinical Project Manager II

    Oct 2024 - now

  • Clinical Project Manager I

    Oct 2021 - Sept 2024

  • Senior Clinical Research Associate / Start-up CRA

    Dec 2020 - Dec 2021

  • Clinical Research Associate

    Dec 2017 - Dec 2021
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  Amgen

  Jan 2018 - Dec 2020

  Clinical Research Associate II / Start-up CRA

  All CRA related activities including:- Preparation, Performing, Follow-up on Evaluation, Initiation, Monitoring and Close-Out Visits;- Investigator Site File/Pharmacy File Review;- Source Data Verification (SDV);- Source Data Review (SDR);- IP Accountability, Return and Destruction;- Communication with all trial related staff (Investigators, Sponsor's Project Team, Pharmacists, Laboratory Staff, External Vendors, Others);- Trial Supplies Management;- Protocol Compliance Verification;- Protocol Deviation Identification, Reporting and Follow-up;- Query Follow-up and Resolution;- Centralized Monitoring;- Risk-Based Monitoring;Therapeutic Areas: Rheumatology, Oncology, Pediatric Oncology, and Cardiology and Pediatric Oncology; Show less