Experience

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  Roche pharmaceuticals

  Oct 2000 - Jun 2002

  Medical manager

  Responsible for developing strategies for medical activities such as: coordinating local and international clinical studies (starting from Phase III), reinforcing the relationship with the physicians integrated with the medical societies and key opinion leaders, providing support for regulatory affairs, call center and pharmacovigilance activities as well as the marketing and sales areas, sales representatives training, participating in the international meetings of the Transplant team and in the main congresses. Show less

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  Wyeth pharmaceuticals

  Jun 2002 - Sept 2004

  Senior medical manager

  Responsible for coordinating and aligning the local medical activities with the global strategy, starting from the moment at which the product reaches phase III of its development with the coordination of the local and international clinical studies. Responsible for the phase IV studies and organizing regional and national symposiums. Support for regulatory affairs, call center and pharmacovigilance activities, generating data and tendencies about the current clinical practice to marketing and sales area. Sales representatives training. Participating in the main congresses related to Gynecology and Obstetrics and in the International Team meetings for the Women’s Health franchise. Reported to Medical Director and VP Medical Affairs. Show less

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  Organon pharmaceuticals

  Sept 2004 - Mar 2007

  Senior medical manager

  Responsible for coordinating and aligning the medical activities, generating data about the current clinical practices and tendencies for the marketing and sales areas, organizing regional and national symposiums, managing the pharmacovigilance area and Balanced Scorecard within the medical department. Technical-scientific assessment of the products being prospected by Business Development department, as well as the development of new products, starting from their formulation through the clinical studies and the dossier for regulatory register. The Brazilian affiliate was the first in the world to launch a 100% locally-developed product. Show less

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  Biogen idec

  Mar 2007 - May 2010

  Associated medical director

  Start up: Implementing the medical department of the Brazilian affiliate of Biogen Idec, having been responsible for obtaining the regulatory approval for Avonex and Tysabri products, for implementing the call center, pharmacovigilance and the entire compliance area, for preparing and managing the technical-scientific training of the sales force and for creating a website for updating and training the same.

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  Aché laboratórios

  Oct 2010 - May 2012

  Executive medical manager

  Responsible for medical affairs area (medical support for marketing area, scientific information, pharmacovigilance, regulatory, clinical research and bioequivalence) having under my responsability 70 people. Direct report to Managing Director.

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  Ferring pharmaceuticals

  May 2012 - Feb 2021

  Close collaboration with the Therapeutic Area (TA) Medical Directors and the overall Global Medical affairs (GMA) team, accountable for the development and roll-out of the GMA Medical Strategy. Integral part of cross-functional teams, working very closely with R&D, Global Marketing and Business Development. Accountable that medical affairs input is provided for (1) Phase II and Phase III study design, (2) the clinical trial investigator selection process, and (3) the planning of future Phase IIIb, Phase IV and Real-World Evidence studies. Help to ensure a leading role for GMA in publication planning and execution for marketed Ferring medicines as well as for those to be launched in the next two years. Also ensure appropriate medical affairs input into the search and evaluation of business development opportunities. Show less

  • Global Medical Director - Medical Strategy

    Dec 2017 - Feb 2021

  • Global Medical Director Urology/Ocology

    Aug 2016 - Feb 2021

  • Country Medical Director

    May 2012 - Jul 2016
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  Biolab sanus farmacêutica

  Feb 2021 - Sept 2022

  Head of medical affairs & clinical development

  Head of clinical development and medical affairs being responsible for design, develop and implement phase I, II, III and IV studies (including RWE) as well as full responsibility for publication planning and execution. As head of medical affairs, I am accountable for medical support for marketing, scientific information, customer service center and pharmacovigilance.

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  Medison pharma

  May 2023 - now

  Medical director brazil & colombia

  Responsible for shaping the development of Brazilian and Colombian medical affairs strategy and support the overall commercial strategy via therapeutic area clinical knowledge and insight from key external experts and stakeholders.• Lead the scientific, medical and data gathering knowledge, identify/interpret the information that is pertinent/relevant to the medical activities. • As an integral part of the local leadership team, be responsible for executing the medical affairs plans and overseeing budget, planning, resource allocation as well as ensure its timely execution.• Leadership of the Country Medical personnel (managers and MSL’s)• Support regulatory, pharmacovigilance, commercial, market access and reimbursement activities in Brazil and additional countries in LATAM.• Establish effective professional engagement with medical communities, opinion leaders, medical societies and other external stakeholders (e.g.: patient advocacy groups, payer organizations and medical government officials).• Lead and support the Implementation of medical education activities, disease awareness programs and various medical affairs activities in conferences and medical associations meetings Show less