Ph3Key Responsibilities /h3ulliPerforms 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. /liliDevelops a deep knowledge of the therapeutic areas covered and the relative market. /liliReports all information about adverse drug effects to the Scientific Service and the companys Pharmacovigilance team in line with current regulations and company procedures. /liliPrepares and plans interviews and meetings with healthcare professionals and tracks relevant information obtained in order to improve the scientific efficacy in subsequent meetings. /liliPerforms 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. /liliConducts non-promotional educational and information activities for healthcare operators (both prescribing and non-prescribing professionals) involved in patient care according to company directives. /liliKnows and applies company procedures for scientific information activities and manages related materials scientific and technological supports /liliSupports company functions in activities aimed at ensuring the correct supply / provision of products. /liliShares relevant information with the Area Manager In Field Team members and colleagues at headquarters to anticipate changes and implement company strategies. /li /ulh3Qualifications : Requirements /h3ulliEducational background as specified in art. 122 paragraph 2 of Legislative Decree 24 / 04 / 2006 No. 219. /liliDeep knowledge of regulatory and ethical requirements related to scientific drug information and where applicable medical devices. /liliHigh professional qualification and adequate scientific product and market knowledge. /liliHigh 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. /liliStrong stakeholder management skills to effectively manage questions and objections. /liliPrevious experience in pharmaceutical / medical devices business. /liliGood knowledge of English both written and spoken. /liliAbility to use IT tools provided by the company. /liliPrevious experience in a matrix organizational environment. /liliCompliance with any other legal requirements as per current regulations and company procedures /li /ulh3Additional Information /h3pAbbVie 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. /ppUS Puerto Rico only - to learn more visit Puerto Rico applicants seeking a reasonable accommodation click here to learn more : /ph3Work /h3pNo /ph3Employment Type /h3pFull-time /ph3Key Skills /h3pSales Experience,Marketing,Customer Service,Communication skills,Military Experience,Retail Sales,Product Demos,Customer Support,Product Management,Product Development,Unity,Microscopy /ph3Experience /h3pyears /ph3Vacancy /h3p1 /p /p #J-18808-Ljbffr