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Crea una Job Alert gratuita per product specialist oncohematology - toscana / firenze

Product Specialist Oncohematology - Toscana

Pubblicato il 03-08-2026 - Abbvie in Firenze

ph3About AbbVie /h3 pAbbVie'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 Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. /p h3Company Description /h3 h3About AbbVie /h3 pAbbVie'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 Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. /p pAbbVie'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 Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. /p h3Job Description /h3 h3Key Responsibilities /h3 ul liPerforms 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.



/li liDevelops a deep knowledge of the therapeutic areas covered and the relative market. /li liReports all information about adverse drug effects to the Scientific Service and the company's Pharmacovigilance team, in line with current regulations and company procedures. /li liPrepares and plans interviews and meetings with healthcare professionals and tracks relevant information obtained in order to improve the scientific efficacy in subsequent meetings. /li liPerforms 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. /li liConducts non-promotional educational and information activities for healthcare operators (both prescribing and non-prescribing professionals) involved in patient care, according to company directives. /li liKnows and applies company procedures for scientific information activities and manages related materials, scientific and technological supports /li liSupports company functions in activities aimed at ensuring the correct supply/provision of products. /li liShares relevant information with the Area Manager, In Field Team members and colleagues at headquarters to anticipate changes and implement company strategies. /li /ul h3Qualifications /h3 ul liEducational background as specified in art. 122 paragraph 2 of Legislative Decree 24/04/2006 No. 219.



/li liDeep knowledge of regulatory and ethical requirements related to scientific drug information and, where applicable, medical devices. /li liHigh professional qualification and adequate scientific, product, and market knowledge. /li liHigh 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. /li liStrong stakeholder management skills to effectively manage questions and objections. /li liPrevious experience in pharmaceutical/medical devices business. /li liGood knowledge of English, both written and spoken. /li liAbility to use IT tools provided by the company. /li liPrevious experience in a matrix organizational environment. /li liCompliance with any other legal requirements, as per current regulations and company procedures. /li /ul h3Additional Information /h3 pYour total reward package at AbbVie will be made up of multiple components, including compensation, well-being and benefits. /p pIn 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. /p pIn this role, you will also be entitled to receive a company car. /p pFull details of our comprehensive package will be shared during the recruitment process. /p pThe national collective bargaining agreement applicable to this position is B011 – CCNL Chemical-Pharmaceuticals Industry. /p pAbbVie 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. /p pUS Puerto Rico only - to learn more, visit /p pUS Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: /p /p #J-18808-Ljbffr

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