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AbbVie

Product Specialist, Rheumatology

AbbVie

Product Specialist in Rheumatology for AbbVie focusing on scientific information activities and healthcare provider interactions. Involved in developing market knowledge and reporting drug effects.

Posted 7/8/2026full-timeRemote • 🇮🇹 ItalyMid-LevelSenior💰 €51,000 - €88,500 per yearWebsite

About the role

Key responsibilities & impact
  • Performs scientific information activities for physicians in accordance with Legislative Decree 24/04/2006 No. 219, the Farmindustria Code of Ethics, regional guidelines on drug scientific information regulations, and, where applicable, Legislative Decree 5 August 2022 No. 137.
  • Develops a deep knowledge of the therapeutic areas covered and the relative market.
  • Reports all information about adverse drug effects to the Scientific Service and the company's Pharmacovigilance team, in line with current regulations and company procedures.
  • Prepares and plans interviews and meetings with healthcare professionals and tracks relevant information obtained in order to improve the scientific efficacy in subsequent meetings.
  • Performs support activities aligned with scientific drug information, manages the reporting and information flows according to company directives with the aim to develop territorial interactions.
  • Updates reports using the company tools.
  • Conducts non-promotional educational and information activities for healthcare operators (both prescribing and non-prescribing professionals) involved in patient care, according to company directives.
  • Knows and applies company procedures for scientific information activities and manages related materials, scientific and technological supports.
  • Supports company functions in activities aimed at ensuring the correct supply/provision of products.
  • Shares relevant information with the Area Manager, In Field Team members and colleagues at headquarters to anticipate changes and implement company strategies.

Requirements

What you’ll need
  • Educational background as specified in art. 122 paragraph 2 of Legislative Decree 24/04/2006 No. 219.
  • Deep knowledge of regulatory and ethical requirements related to scientific drug information and, where applicable, medical devices.
  • High professional qualification and adequate scientific, product, and market knowledge.
  • High active listening skills towards the counterpart and ability to ask open-ended questions to understand their scientific needs.
  • Strong communication skills to modulate the style based on the role, profile, and needs of the counterpart.
  • Strong stakeholder management skills to effectively manage questions and objections.
  • Previous experience in pharmaceutical/medical devices business.
  • Good knowledge of English, both written and spoken.
  • Ability to use IT tools provided by the company.
  • Previous experience in a matrix organizational environment.
  • Compliance with any other legal requirements, as per current regulations and company procedures.

Benefits

Comp & perks
  • life assurance
  • medical plan
  • flexible benefits
  • company car

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
Regulatory KnowledgeMarket KnowledgePharmacovigilance ReportingScientific Information ManagementEducational Activity Planning
Soft Skills
Active ListeningStrong CommunicationOpen-Ended Questioning