
Product Specialist, Dermatology
Posted May 24

Posted May 24
This is a fully remote position, open to applicants in Italy.
• Executes scientific information tasks for physicians in compliance with Legislative Decree 24/04/2006 No. 219, the Farmindustria Code of Ethics, regional guidelines on drug scientific information regulations, and, when applicable, Legislative Decree 5 August 2022 No. 137.
• Cultivates an in-depth understanding of the therapeutic areas involved and the associated market.
• Communicates all details regarding adverse drug reactions to the Scientific Service and the company's Pharmacovigilance team, adhering to current regulations and internal procedures.
• Organizes and schedules interviews and meetings with healthcare professionals, documenting pertinent information gathered to enhance scientific effectiveness in future interactions.
• Engages in support activities aligned with scientific drug information, overseeing reporting and information flows in accordance with company guidelines to foster regional interactions.
• Updates reports utilizing company tools.
• Delivers non-promotional educational and informational initiatives for healthcare providers (both prescribing and non-prescribing professionals) involved in patient care, following company directives.
• Understands and implements company protocols for scientific information activities and manages related materials and scientific and technological resources.
• Assists company functions in activities focused on ensuring the appropriate supply and provision of products.
• Shares pertinent information with the Area Manager, In Field Team members, and colleagues at headquarters to anticipate changes and execute company strategies.
• Minimum of 1 year of experience in oncology.
• Educational qualifications as outlined in art. 122 paragraph 2 of Legislative Decree 24/04/2006 No. 219.
• Comprehensive knowledge of regulatory and ethical standards pertaining to scientific drug information and, where applicable, medical devices.
• High level of professional qualification along with sufficient scientific, product, and market knowledge.
• Excellent active listening skills and the ability to pose open-ended questions to comprehend scientific needs.
• Strong communication abilities to adjust the style based on the role, profile, and needs of the counterpart.
• Proficient stakeholder management skills to effectively address questions and objections.
• Prior experience in the pharmaceutical/medical devices sector.
• Proficient in English, both written and spoken.
• Capability to utilize IT tools provided by the company.
• Previous experience within a matrix organizational structure.
• Adherence to any additional legal requirements as per current regulations and company procedures.
• Health insurance.
• Paid time off.
• Professional development.
DentalMonitoring
AbbVie
Harvey
AbbVie
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