Scientific Information Specialist HCV
2 settimane fa
**Job Description**
As a Scientific Information Specialist HCV, you will be responsible for performing 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.
**Key Responsibilities:**
- Develop a deep knowledge of the therapeutic areas covered and the relative market.
- Report all information about adverse drug effects to the Scientific Service and the company's Pharmacovigilance team, in line with current regulations and company procedures.
- Prepare and plan interviews and meetings with healthcare professionals and track relevant information obtained in order to improve the scientific efficacy in subsequent meetings.
- Perform support activities aligned with scientific drug information, manage the reporting and information flows according to company directives with the aim to develop territorial interactions.
- Update reports using the company tools.
- Conduct non-promotional educational and information activities for healthcare operators (both prescribing and non-prescribing professionals) involved in patient care, according to company directives.
- Know and apply company procedures for scientific information activities and manage related materials, scientific and technological supports.
- Support company functions in activities aimed at ensuring the correct supply/provision of products.
- Share relevant information with the Area Manager, In Field Team members and colleagues at headquarters to anticipate changes and implement company strategies.
**Qualifications Requirements:**
- 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.
**Additional Information:**
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.
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