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Maite Buxens

Maite Buxens

Scientific consultant and Medical affairs

Talento
Madrid, Madrid0Miembro desde 6 de diciembre de 2023
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Sobre mí

Several years working on project management in medical/scientific departments (digital, consumer healthcare, pharma). Responsible of medical science projects (implementation and management end-to end), including medical writing, innovation and strategy. Expertise in content generation with strong conceptualization skills targeted to different audiences and communicated through different channels (consumers, patients, HCPs) such as edetailing, infographics, posters, videos, platforms, webinars).

Experience in managing relationships with clients in several geographies and in creating expert networks for several activities (KOL engagement, Advisory Boards, webinars).

Interested in projects related with digital health.

Ability to work independently and to collaborate and interact efficiently (inhouse and with providers and collaborators) with other profiles/departments (e.g., regulatory, marketing, communication, designers) for the development of activities and strategies.

Proactive, good with multi-tasking, with high capacity to solve problems independently.

Experiencia

Nov 2018-Present.

Medical

Science, Manager.

Scientific Excellence

Platform,

SPRIM, Spain.

  • 20176-2018.

Project

Manager in Scientific and Regulatory Affairs, SPRIM, Spain.

  • 20176-2018. Consultant in Scientific and Regulatory Affairs, SPRIM, Spain.
  • 2015-2016. Regulatory and Scientific Affairs Consultant (implant in Abbott and

Aristo Pharma Iberia), McCrowley & Hughes (PharmaLex), Spain.

  • 2015.

Regulatory Affairs

Internship, Sylentis (Zeltia Group), Spain.

  • 2014-2015.

Freelancer: generation of scientific content, LUCA, Spain.

  • 2012-2013.

Postdoctoral Research

Associate, ODU, VA, EE.UU.

  • 2005-2011.Predoctoral Researcher, Dpt. Biochemistry and Molecular Biology,

(UPV/EHU), Spain.

Educación

  • Digital Mindset: Innovation and leadership in the digital era, IESE, 2021.
  • Master in Regulatory Affairs in medicinal products, IUCT, 2015.
  • Biomedicine, Biotechnology and Law, Expert Course, UNED, 2012.
  • Ph.D. Biochemistry and Molecular Biology, UPV/EHU, 2011.
  • Graduated in Biochemistry, UPV/EHU, 2005.

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