As Medical Affairs Manager in Italy, you are the scientific expert for the BU, shaping local/EMEA medical strategy and ensuring evidence-based engagement with HCPs, HCOs, and scientific bodies.
You build trusted medical partnerships to support wound closure and biosurgery, guide clinical strategy, and drive compliant medical communications.
You work cross-functionally to generate evidence, support launches, and reflect risk-agevolazioni in medical materials.
This role offers meaningful impact on patient care and Italy's surgical medical voice.annual bonusparental leave for 12 weeksinsurance plansImplement BU medical strategy through local field activities in collaboration with stakeholdersServe as the local resource for medical and scientific information to HCPs, HCOs, and external stakeholdersEstablish and nurture peer-to-peer relationships with HCPs and KOLsDevelop strategic partnerships with scientific stakeholders and other partnersConceive and lead advisory boards and expert meetings as neededSupport identification and development of KOLs across BU/Surgery areasProvide medical support for launch and development of BU productsSupport evidence generation projects and local clinical research/education initiativesReview and approve medical materials ensuring accuracy and regulatory complianceSupport local teams in addressing HCP inquiries and research constraintsGather insights from HCPs and external researchSupport Professional Education partnerships and charitable contribution processesCollaborate with EMEA Medical Safety & Quality to manage safety inquiries and investigationsKeep updated on scientific advances & evolving healthcare trendsMD degree with specialty (preferably surgical)2-4 years in Medical Affairs, Clinical Affairs, or related scientific xysqume role in medical devices or pharmaKnowledge of clinical research, evidence generation, and medical complianceExperience engaging with HCPs and KOLs in a non-promotional mannerStrong analytical, public speaking, and presentation skillsAbility to work in cross-functional, matrixed environmentsSolid understanding of Italian healthcare system and regulationsPreferred: experience in surgery, clinical trial management or post-market studies, product launches/lifecycle in medical affairs, familiarity with European medical device regulations and clinical evaluation#J-*****-Ljbffr
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