Remotery

Product Specialist, Rheumatology

atAbbVieIT flagItalyFull-timeProduct SpecialistMid-levelSenior€51k – €88.5k/year

Posted 8 hours ago

This is a fully remote position, open to applicants in Italy.

📋 Description

• Executes scientific information tasks for physicians in compliance with Legislative Decree 24/04/2006 No. 219, the Farmindustria Code of Ethics, regional guidelines on scientific drug information regulations, and, where applicable, Legislative Decree 5 August 2022 No. 137.

• Cultivates an extensive understanding of the therapeutic areas involved and the corresponding market.

• Communicates all details regarding adverse drug reactions to the Scientific Service and the company's Pharmacovigilance team, adhering to existing regulations and company protocols.

• Organizes and schedules interviews and meetings with healthcare professionals while documenting pertinent information gathered to enhance scientific effectiveness in future engagements.

• Conducts supportive activities aligned with scientific drug information, oversees reporting and information flows according to company guidelines to foster regional interactions.

• Updates reports utilizing company resources.

• Engages in 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 procedures for scientific information activities and manages associated materials, scientific, and technological resources.

• Assists company functions in activities aimed at ensuring the proper supply and provision of products.

• Shares pertinent information with the Area Manager, In Field Team members, and colleagues at headquarters to foresee changes and execute company strategies.


⛳️ Requirements

• Educational qualifications as stipulated in art. 122 paragraph 2 of Legislative Decree 24/04/2006 No. 219.

• Comprehensive knowledge of regulatory and ethical standards related 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 abilities towards counterparts and the capacity to pose open-ended questions to comprehend their scientific requirements.

• Strong communication skills to adjust the style based on the role, profile, and needs of the counterpart.

• Robust stakeholder management skills to effectively address inquiries and objections.

• Previous experience in the pharmaceutical or medical devices sector.

• Proficient in English, both written and spoken.

• Competence in utilizing IT tools provided by the company.

• Prior experience in a matrix organizational structure.

• Adherence to any additional legal obligations in accordance with current regulations and company procedures.


🏝️ Benefits

• Life assurance

• Medical plan

• Flexible benefits

• Company car

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