Product Specialist, Gastroenterology

Role Overview

• 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.

Benefits

• Health insurance
• 401(k) matching
• Flexible work hours
• Paid time off