BrightOwl Loader Loading


Current Experience

  • Study Coordinator, Oncology
    Since April 2016
    Study coordinator of phase II and phase IIIb clinical trials; Participation in screening and randomization of patients; Organization and participation in monitoring visits to Center; Query resolution and data entry in different eCRF's: iMEDIDATA, MEDIDATA RAVE and INFORM; Support to Principal Investigators and CRA´s monitors in their activities; Collection, recording and processing of clinical data; Update and management of documents and files required for clinical trials; Medication dispensing through ClinPhone platform; Preparation of investigator initiative projects for submission to the Centro Hospitalar Lisboa Norte´s Ethics Committee; ICH-GCP Guidelines.

Past Experience

  • Clinical Project Assistant, Oncology
    September 2014 --- March 2016
    Assist the Studies Coordinatores in the management of clinical trials; Assist in the management of Case Report Forms (CRFs) and clinical data query resolution; Assist the team with accurately updating and maintaining clinical system – MEDIDATA; Assist the clinical team in the updating and management of clinical documents and reports; Clinical data manager of retrospective studies: “Relative effectiveness of aromatase inhibitors versus tamoxifen in patients with early breast cancer.” “Standards and treatment outcomes in patients with breast cancer with less than 1 cm (T1a-bN0M0).” “Treatment patterns and outcomes among patients with HER2+ disease among the ROR-SUL.” Record, analyze, and update the clinical and pathological characteristics, treatment patterns and clinical outcome in patients with breast cancer; Data entry and Management of ROR platform at Hospital Santa Maria; Participation in external audits to evaluate the quality of clinical registration performed by others institutions - Registo Oncológico Regional-Sul;

  • Funding Programs Assistant
    May 2013 --- August 2014
    - Assists obtaining funding for entrepreneurial projects. - Provides assistance in all steps involved in the process of grant management (proposal preparation, submission, negotiation). - Preparation of scientific research projects for submission to the Centro Hospitalar Lisboa Norte´s Ethics Committee. - Manager of ProQuest Pivot data base.


Self Assessment :
AdaptabilityAnalytical thinkingAttention to detailCollaborationFlexibilityOrganizationProactivityResponsibility


Self Assessment :
Clinical Data ManagementCancerClinical trialsPharmaceutical SciencespharmacologyPharmacovigilanceProject ManagementBiomedical SciencescGMPClinical Data Management (CDM)Clinical study reportsCRFData ManagementeCRF
LinkedIn Assessment :
Clinical Data ManagementClinical trialsProject ManagementoncologyBreast CancerClinical researchPharmaceutical IndustryHematologyClinical Data AnalystImmunologyMicrobiologyBiochemistryData entryResearch Fundingmolecular biologyBiotechnologyTeamwork


  • Master's degree in Student of Pharmaceutical Sciences from Faculdade de Farmácia da Universidade de Lisboa in 2016
  • University Degree in Biomedical Science Laboratory from Escola Superior de Tecnologia da Saúde de Lisboa in 2012
  • University degree in Biomedical Science Laboratory from Università degli Studi di Verona in 2012

Training and Certification

  • Clinical Research Course to Study Nurses and Study Coordinators Certification
  • Curso Intensivo de Farmacovigilância Certification
  • Investigator Site Personnel ICH GCP Training Certificate Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Professional Proficiency

Area / Region

Lisbon, Portugal


Driving License
  • Yes