14 ott - Pomezia
Experteer Italy
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-benefit in medical materials.
This role offers meaningful impact on patient care and Italy's surgical medical voice.
annual premio
parental leave for 12 weeks
insurance plans
Implement BU medical strategy through local field activities in collaboration with stakeholders
Serve as the local resource for medical and scientific information to HCPs, HCOs, and external stakeholders
Establish and nurture peer-to-peer relationships with HCPs and KOLs
Develop strategic partnerships with scientific stakeholders and other partners
Conceive and lead advisory boards and expert meetings as needed
Support identification and development of KOLs across BU/Surgery areas
Provide medical support for launch and development of BU products
Support evidence generation projects and local clinical research/education initiatives
Review and approve medical materials ensuring accuracy and regulatory compliance
Support local teams in addressing HCP inquiries and research constraints
Gather insights from HCPs and external research
Support Professional Education partnerships and charitable contribution processes
Collaborate with EMEA Medical Safety & Quality to manage safety inquiries and investigations
Keep updated on scientific advances & evolving healthcare trends
MD degree with specialty (preferably surgical)
2-4 years in Medical Affairs, Clinical Affairs, or related scientific xysqume role in medical devices or pharma
Knowledge of clinical research, evidence generation, and medical compliance
Experience engaging with HCPs and KOLs in a non-promotional manner
Strong analytical, public speaking, and presentation skills
Ability to work in cross-functional, matrixed environments
Solid understanding of Italian healthcare system and regulations
Preferred: 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
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