Neuroscience Medical Information Specialist

AbbVie Inc.

Roma

Sur place

EUR 45 000 - 60 000

Plein temps

Il y a 7 jours
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Résumé du poste

AbbVie is seeking a scientifically minded professional in Italy to perform non-promotional information activities for physicians and healthcare professionals while ensuring compliance with local regulations and ethical standards.

You will develop deep therapeutic area knowledge, manage information flows, and collaborate with the Scientific Service and Pharmacovigilance teams to maintain high-quality, compliant scientific communications.

Qualifications

  • Knowledge of regulatory and ethical requirements for scientific drug information.
  • Experience with pharmaceutical/medical devices.
  • Good English, written and spoken.
  • Ability to use IT tools provided by the company.
  • Experience in a matrix organizational environment.
  • Compliance with legal requirements.

Responsabilités

  • Performs scientific information activities for physicians following applicable laws and codes.
  • Develops deep knowledge of therapeutic areas and related market dynamics.
  • Reports adverse drug information to Scientific Service and Pharmacovigilance teams.
  • Prepares and plans interviews and meetings with healthcare professionals.
  • Manages information flows and updates reports to improve scientific efficacy.
  • Conducts non-promotional educational activities for healthcare operators per company directives.
  • Supports product supply/provision and shares information with Area Manager and HQ.

Connaissances

Regulatory knowledge
Scientific knowledge
English proficiency
Stakeholder management
Communication skills
Pharma experience
IT literacy
Matrix organization

Description du poste

AbbVie is seeking a scientifically minded professional in Italy to perform non-promotional information activities for physicians and healthcare professionals while ensuring compliance with local regulations and ethical standards.

You will develop deep therapeutic area knowledge, manage information flows, and collaborate with the Scientific Service and Pharmacovigilance teams to maintain high-quality, compliant scientific communications.

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