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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

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