FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
About the role
Key responsibilities & impact- Performs 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
- Develops a deep knowledge of the therapeutic areas covered and the relative market
- Reports all information about adverse drug effects to the Scientific Service and the company's Pharmacovigilance team, in line with current regulations and company procedures
- Prepares and plans interviews and meetings with healthcare professionals and tracks relevant information obtained in order to improve the scientific efficacy in subsequent meetings
- Performs 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
- Conducts non-promotional educational and information activities for healthcare operators (both prescribing and non-prescribing professionals) involved in patient care, according to company directives
- Knows and applies company procedures for scientific information activities and manages related materials, scientific and technological supports
- Supports company functions in activities aimed at ensuring the correct supply/provision of products
- Shares relevant information with the Area Manager, In Field Team members and colleagues at headquarters to anticipate changes and implement company strategies
Requirements
What you’ll need- At least 1 year of experience in oncology
- 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 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
Benefits
Comp & perks- Health insurance
- 401(k) matching
- Flexible work arrangements
- Professional development
- Paid time off
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
oncology experiencescientific drug informationpharmacovigilanceregulatory complianceethical requirementsmarket knowledgeeducational background in scientific fieldsreporting skillsnon-promotional educational activitiesterritorial interactions
Soft Skills
active listeningopen-ended questioningstrong communicationstakeholder managementadaptabilityinterpersonal skillscollaborationproblem-solvingorganizational skillsstrategic thinking
Certifications
Legislative Decree 24/04/2006 No. 219Legislative Decree 5 August 2022 No. 137