Emea Senior Medical Advisor/Medical Education Lead Cardiovascular

Overview At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https : / / Job Details Job Function: Medical Affairs Group: Medical Affairs – MD Job Category: People Leader All Job Posting Locations: Beerse, Antwerp, Belgium; Beirut, Lebanon; Breda, Netherlands; Budapest, Hungary; Espoo, Uusimaa, Finland; Issy-les-Moulineaux, France; Madrid, Spain; Milano, Italy; NEUSS, Germany; Oslo, Norway; Pefki, Attiki, Greece; Porto Salvo, Portugal; Prague, Czechia; Warsaw, Masovian, Poland; Wien, Austria; Zagreb, Grad Zagreb, Croatia Responsibilities Lead the collaboration, support, and communication between the Regional Medical Affairs Team for a specific product or group of products and a specific group of Operating Company Medical Affairs Teams including OpCos, as well as Global cross-functional members / R&D. Create, build and nurture a trusted collaboration with the external scientific community to facilitate continuous communication, influence and transfer of knowledge between the company, thought leaders and a wider group of physicians and customers. Support, follow up and/or execute the implementation of activities as outlined in the EMEA Medical Affairs Product Plan across EMEA under the guidance of the EDTL in close cooperation with operating companies and other EMEA functions (EMPL, SKL, MESRL, Regulatory Affairs, Marketing, HEMAR). Shape and input into the development of the EMEA Medical Strategy and the EMEA MAP Plan for a specific product or group of products, aligned with Global strategy and IBVT; anticipate needs and identify gaps; incorporate feedback from external scientific communities. Co-create the development of the Global Medical Strategy, CATs, WWIEGP and Launch Readiness plans for a product or group of products. Represent the unified EMEA MAF voice to internal and external stakeholders; coordinate and execute on EMEA-level medical education plan. Shape and execute the Launch Readiness Plan framework for new products or indications in collaboration with countries and global teams. Drive cross-functional accountability for initiatives spanning indications, therapeutic areas, and strategic alliances; align and execute across diverse teams and geographies. Leverage advanced technologies, digital platforms, and data-driven insights to inform medical strategies and decision-making; foster collaboration with global, regional, and local partners. Champion adoption and integration of new technologies to enhance medical engagement, evidence generation, and knowledge dissemination. Foster and manage complex collaborations with alliance partners, academic institutions, and external stakeholders to co-develop innovative medical solutions addressing unmet patient needs. Act as a scientific expert with external thought leaders; build networks with external experts and patient groups. Main Activities / Tasks EMEA Medical Affairs Product Team Core Membership: act as an EMEA MA expert, shape strategy for designated product(s), represent EMEA voice, develop product knowledge, and maintain external thought leader networks. Provide expertise to the Medical Affairs Functional Network and Operating Company functions; input into the EMAP Team charter and support implementation of the EMEA MA Strategy and Plan. Collaborate with the EMAP Team to shape and gather insights for the EMEA Medical Affairs Product Plan; drive implementation of Strategy, Plan, and Medical Education Strategy. Lead Launch Readiness efforts alongside EDTL; ensure effective communications between EMAPT and local MA teams to minimize duplication and coordinate across teams. Assist in designing local publications plans and input into Medical Education plans in EMEA; provide scientific input into Diagnostics, Biomarker, and Devices strategies if applicable. Support operating companies in developing, aligning, and implementing product strategies and tactical plans; generate impactful patient and business outcomes. Identify and address opportunities and challenges with limited EDTL oversight. External Relationships: build trusted collaborations with external scientists to inform product strategy and protocols; translate relationships into tangible projects. Study Planning and Execution: build MAF study plans and evaluate IIS proposals for alignment with medical strategy; oversee EG activities with EMPL and MADU. Publications: support development and implementation of the EMEA MA publication plan; ensure compliance with J&J guidelines and policy; ensure EMEA messages reflect scientific data. Medical Education: shape pan-EMEA Medical Education programs, review proposals, and support materials with SKL; rehearse with speakers. Other Activities: contribute to EMEA business development; collaborate with late lifecycle management for medical input; liaise with R&D as needed. Compliance: ensure safety reporting requirements are met according to policies and SOPs; ensure regulatory and legal requirements are understood and complied with in planning and contracting. Essential Knowledge & Skills Deep knowledge of atrial fibrillation and/or stroke with a proven external expert network. Strong knowledge of all products within the Therapeutic Area; clinical trial design and data analysis experience; EU CTD and GCP knowledge; study execution and regulatory affairs familiarity. Customer and market focus with emphasis on business results; strategic thinking; ability to lead in a complex, changing environment. Excellent communication and influencing skills; ability to work in a matrix environment; ability to travel within EMEA and internationally. Fluency in English required; additional EMEA languages a plus. Experience Advanced scientific or medical degree. 4+ years in an area relevant to the TA; 5+ years in medical affairs, including medical education at regional level. Experience in alliance environments is a plus; Local Operating Company experience required. Job Location: The role is EMEA based and is likely to involve extensive travel. The role holder should be based in their country of residence with access to travel via a J&J office. Required Skills Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Developing Others, Healthcare Trends, Inclusive Leadership, Leadership, Medical Affairs, Medical Communications, Medical Compliance, Product Strategies, Quality Assurance (QA), Research Proposals, Stakeholder Management, Strategic Thinking, Team Management J-18808-Ljbffr EMEA Senior Medical Advisor—Medical Education Lead (Cardiovascular) • Turbigo, Lombardy, ITALY #J-18808-Ljbffr