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Product Specialist, Neuroscience
AbbVie. Perform scientific information activities for physicians in accordance with Italian legislation, the Farmindustria Code of Ethics, regional guidelines, and applicable company procedures .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates deep knowledge of regulatory and ethical requirements related to scientific drug information, along with strong communication and stakeholder management skills. Capable of conducting educational activities and managing information flows in compliance with company procedures.
Highest-signal resume keywords
Regulatory And Ethical RequirementsScientific Drug InformationStakeholder ManagementPharmaceutical/Medical Devices ExperienceEnglish Proficiency
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Scientific Information ActivitiesAdverse Drug Effect ReportingMarket KnowledgeEducational Activity PlanningInformation Flow Management
Soft Skills
Active ListeningStrong CommunicationOpen-Ended QuestioningAdaptability
Tools & Technologies
Company IT Tools
Certifications & Qualifications
Educational Background As Specified In Art. 122 Paragraph 2 Of Legislative Decree 24/04/2006 No. 219
Industry Keywords
PharmaceuticalMedical DevicesComplianceFarmindustria Code Of EthicsMatrix Organizational Environment
About the role
Key responsibilities & impact- Perform scientific information activities for physicians in accordance with Italian legislation, the Farmindustria Code of Ethics, regional guidelines, and applicable company procedures
- Develop deep knowledge of covered therapeutic areas and the related market
- Report adverse drug effects to the Scientific Service and Pharmacovigilance team
- Prepare and plan interviews and meetings with healthcare professionals
- Track information from meetings to improve scientific efficacy in subsequent interactions
- Perform support activities related to scientific drug information and manage reporting and information flows
- Update reports using company tools
- Conduct non-promotional educational and information activities for healthcare operators involved in patient care
- Apply company procedures for scientific information activities and manage related materials and scientific/technological supports
- Support company functions in ensuring the correct supply/provision of products
- Share relevant information with the Area Manager, In Field Team members, and headquarters colleagues
- Anticipate changes and implement company strategies
Requirements
What you’ll need- 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 and ability to ask open-ended questions
- Strong communication skills to adapt style based on the counterpart's role, profile, and needs
- Strong stakeholder management skills to manage questions and objections
- Previous experience in pharmaceutical/medical devices business
- Good knowledge of English, written and spoken
- Ability to use company-provided IT tools
- Previous experience in a matrix organizational environment
- Compliance with applicable legal requirements and company procedures
- Willingness/ability to travel 75% of the time
Benefits
Comp & perks- Base pay and incentive as per local policy
- Life assurance
- Medical plan
- Flexible benefits
- Company car
- Comprehensive total reward package
- National collective bargaining agreement: B011 – CCNL Chemical-Pharmaceuticals Industry