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Experiences

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. 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.

Personality

Self Assessment :
AdaptabilityAnalytical thinkingAttention to detailCollaborationFlexibilityOrganizationProactivityResponsibility

Knowledge

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

Education

  • 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 in 0000 Certification
  • Curso Intensivo de Farmacovigilância in 0000 Certification
  • Investigator Site Personnel ICH GCP Training Certificate in 0000 Certification

Languages

BrightOwl Assessment:
Self Assessment:
Portuguese
Native
English
Professional Proficiency
Spanish
Professional Proficiency

Area / Region

Lisbon, Portugal

Others

Driving License
  • Yes

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