Product Specialist Dermatology - Toscana, Umbria

AbbVie; Prato; Vor Ort; EUR 51.000 - 89.000; Vollzeit

Benefits dieser Stelle

Company car

Life assurance

Medical plan

Zusammenfassung

AbbVie in Italy (Toscana/Umbria) is seeking a Product Specialist in Dermatology to drive scientific information activities and develop deep knowledge of therapeutic areas in a full-time role with 100% travel. The position requires strong regulatory/ethical understanding, high qualification, and excellent communication.

English proficiency is required. The role includes reporting safety information, engaging with healthcare professionals, and supporting education and product provision while

Qualifikationen

• Regulatory and ethical knowledge for scientific drug information is required.
• High qualification level with solid product, market knowledge.
• Excellent communication and stakeholder management skills.
• Good command of English, written and spoken.

Aufgaben

• Conduct scientific information activities for physicians according to Italian regulations.
• Develop deep knowledge of therapeutic areas and market.
• Report adverse drug effects to Pharmacovigilance per regulations.
• Plan interviews/meetings with healthcare professionals and capture insights.
• Support non-promotional educational activities for healthcare operators.
• Share information with Area Manager and HQ to inform strategy.
• Ensure correct supply/provision of products and updates in reports.

Kenntnisse

Strong communication skills

Active listening

Stakeholder management

English proficiency

Team collaboration

Ausbildung

Educational background as specified in art. 122 paragraph 2 of Legislative Decree 24/04/2006 No. 219

Jobbeschreibung

Product Specialist Dermatology - Toscana, Umbria

• Full-time
• Therapy Area: Immunology
• Workday Global Grade: 15
• Travel: Yes, 100% of the Time
• Compensation: EUR 51,000 - EUR 88,500 - yearly

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.

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.

• 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.

Your total reward package at AbbVie will be made up of multiple components, including compensation, well-being and benefits.
In this role, you will receive base pay and incentive as per the local policy. You will also receive a number of benefits including life assurance, medical plan, flexible benefits, etc.

In this role, you will also be entitled to receive a company car.

Full details of our comprehensive package will be shared during the recruitment process.

The national collective bargaining agreement applicable to this position is B011 – CCNL Chemical-Pharmaceuticals Industry.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.