Key Responsibilities: 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: Minimum of 1 year of experience in a Product Specialist role 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.
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