Product Specialist – Oncohematology

AbbVie

Product Specialist in Oncohematology for AbbVie discovering and delivering innovative therapies. Engaging healthcare professionals while adhering to regulatory compliance and scientific integrity.

Posted 7/24/2026full-timeRemote • 🇮🇹 ItalyMid-LevelSenior💰 €51,000 - €88,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates deep knowledge of regulatory and ethical requirements related to scientific drug information, along with strong communication and stakeholder management skills. Proficient in conducting educational activities for healthcare professionals and managing information flows in compliance with company directives.

Highest-signal resume keywords

Regulatory CompliancePharmaceutical KnowledgeStakeholder ManagementScientific CommunicationAdverse Drug Reporting

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Scientific Information ActivitiesPharmacovigilanceMarket KnowledgeEducational ActivitiesIT Tool Proficiency

Soft Skills

Active ListeningOpen-Ended QuestioningCommunication Skills

Tools & Technologies

Company Reporting Tools

Industry Keywords

Legislative Decree 24/04/2006 No. 219Farmindustria Code of EthicsMedical DevicesMatrix Organizational Environment

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