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Current Experience

  • Scientific Advice Trainee
    Since October 2016

Past Experience

  • Scientific Affairs Junior Officer
    April 2015 --- September 2016

    • Preparation of Non-Clinical and Clinical Reports (modules 2.4, 2.5, 2.6 and 2.7 of the CTD), in accordance with the most up-to-date good practices and assuring a consistent bibliographic support;
    • Development of Environmental Assessment (ERA) Reports (module 1.6 of the CTD);
    • Development and revision of Summary of Product Characteristics (SmPC), Labelling and Package Information Leaflets (PIL);
    • Preparation of Readability User Testing Reports (Complete or Bridging Reports);
    • Answering to LoDs that may arise from the Authorities in what concerns to the modules mentioned above;
    • Preparation of meeting reports, such as advisory boards;
    • Answering to scientific information requests regarding medicinal products.

  • Technical Services Trainee
    January 2015 --- March 2015

    • Development of Data Compilation Protocols and Master Batch Records for the Tech Transfer of new injectable pharmaceutical products based on Technical Data from the current manufacturers or Development Reports from R&D departments;
    • Training in the relevant departments of the plant: Compounding, Production, Quality Assurance, Packaging, Maintenance, QC.

  • Trainee
    January 2014 --- June 2014
    - Promotion of the rational use of medicines, dermocosmetic counselling and selling; Stocks management and reception of Medicines; - Pharmacotherapeutical counselling and organisation of the patient's weekly medication; - Determination of biochemical parameters, such as glycaemia, total cholesterol and blood pressure.

  • Trainee
    July 2013 --- August 2013


Self Assessment :
AdaptabilityCollaborationCompetitivenessCuriosityEfficiencyFlexibilityIndependenceReaction to stressResiliencyResponsibilityService orientedSociability


Self Assessment :
Scientific writingClinical trialsCompliance with regulationsEMAMedical affairsMedical writingPharmaceutical IndustryRegulatory affairsSearch literature on clinical trials
LinkedIn Assessment :
Scientific AffairsRegulatory affairsMedical writingReadabiltyLabelingTeam Work

Skills and Expertise

Self Assessment :
Interpret data Report data Search literature on clinical trialsCapture data on source documentsClinical data collectionConduct literature searchesCreate clinical documentsInterpret scientific dataRegulatory documentationWriting regulatory documents


  • Callan Intensive - Callan Method English Classes in General english from Callan School London in 2014
  • Master of Science (MSc) in Pharmaceutical Sciences from University of Coimbra – Faculty of Pharmacy in 2014
  • General English (B2 level according to CEFR for languages) in from University of Coimbra - Faculty of Arts and Humanities in 2012


BrightOwl Assessment:
Self Assessment:
Professional Proficiency

Work Preferences

  • Notice Period:
    2 weeks
  • Positions I am interested in:
    Clinical Research Consultant Clinical Trial Assistant (CTA) Regulatory Affairs Associate
  • Locations I am interested in:
    Belgium Denmark London, United Kingdom Netherlands
  • Work From Home:
  • Work Regime:
    Permanent position
  • International:

Area / Region

London, United Kingdom


Driving License
  • Yes