Director medical affairs strategic markets emea - electrophysiology (m/f/d)

Ph3Experteer Overview /h3pIn this role you will lead Medical Affairs for Electrophysiology across the G5 markets, shaping medical strategy and ensuring regulatory alignment. You’ll oversee the MSL team, translate clinical insights into franchise priorities, and drive patient‑centric medical leadership. You’ll collaborate with cross‑functional teams to advance EP solutions, manage safety and regulatory inputs, and influence strategic decisions. This is a high‑impact opportunity to steer innovation in cardiovascular care across Europe, aligning science with market needs. /ph3Retribuzione / Benefits /h3ulliOversee MSL work for Electrophysiology in G5 markets (DE, FR, UK, IT, ES) and ensure cohesive medical input into strategy /liliProvide procedural insights and translate opportunities to address unmet surgical needs for franchise innovation /liliEnsure knowledge transfer from global medical to G5 markets and contribute to Target Product Profiles /liliLead safety oversight across end‑to‑end processes, including adverse event reporting and health hazard evaluations /liliCritically evaluate clinical risk and provide evidence‑based risk‑benefit determinations /liliProvide medical input for patient safety decisions and regulatory submissions with EMA and other regulators /liliDevelop and implement clinical evidence strategy and lead education and training initiatives /liliManage MSL operational aspects (budget, performance, succession) and coach team members /liliFoster external engagement with KOLs, physicians, academic institutions, and regulators; represent customer perspective in strategic discussions /li /ulh3Responsabilità /h3ulliMedical degree (MD); advanced degree (PhD, PharmD) highly preferred /lili12+ years in medical affairs or related roles within medical device/pharma with leadership experience /liliClass III Medical Device experience /liliExtensive EP clinical practice experience and AFib expertise /liliStrong knowledge of clinical trial design, regulatory requirements, and healthcare compliance /liliExperience with EMA interactions and health authority submissions /liliProven ability to lead cross‑functional teams in a complex matrix organization /liliExcellent communication and stakeholder management skills /li /ulh3Requisiti fondamentali /h3ulliannual bonus /lilivacation days /liliparential leave (min 12 weeks) /lilibereavement leave /lilicaregiver leave /lilivolunteer leave and wellbeing reimbursement /li /ul /p #J-18808-Ljbffr