Clinical Development Lead- Cardiovascular

Clinical Development Lead- Cardiovascular: Clinical Strategy /General Clinical Trials / Medical Device study Background: Are you ready to shape the future of healthcare by leading the clinical development strategy for next generation diagnostic solutions? As a Clinical Development Lead, Cardiovascular and metabolic diseases (CVMD) within our Clinical and Medical Affairs organisation in Diagnostics, you will play a pivotal role in planning and implementing clinical development activities that bring medically-differentiated solutions to patients globally. In this role, you will act as a senior strategic voice and trusted advisor, fostering an environment where science and collaboration thrive. Key Responsibilities: Drive Clinical Strategy: Lead the clinical development strategy for large-scale studies and complex programs, in the CVMD area, defining clinical utility, intended use, and claim extensions across our portfolio. Lead Health Authority Interactions: Work closely with Global Regulatory Affairs in the completion and submission of global regulatory filings, authoring critical sections of meeting packages and reviewing clinical documents for international regulatory submissions. Forge Stakeholder Partnerships: Act as the medical lead in external interactions with health authorities, build strategic relationships with international Key Opinion Leaders (KOLs), and drive development partnerships across industry and academia. Foster Communication Excellence: Oversee the implementation of communication strategies for clinical studies, representing the organisation at major medical congresses, advisory boards, and in key publications. Champion Innovation & Excellence: Act as a key driver for competitive differentiation,



innovation, and early pipeline activities while developing intellectual property strategies and optimising clinical processes. Coach and Mentor: Act as a dedicated coach for team members, nurturing confidence and helping colleagues develop their skills and expertise. Must Haves: Medical degree (MD) or an advanced degree (PhD) in cardiology, metabolic diseases, obesity or related fields. Established experience within academia, diagnostics, or the pharmaceutical industry, in the CVMD area. Clinical Expertise: Proven track record in In Vitro Diagnostics (IVD) or Medical Device study management across all stages of global clinical trials, including protocol design and report writing. Program Leadership: Demonstrated experience leading large, complex development programs and guiding cross-functional, matrixed teams. Regulatory Knowledge: Deep understanding of applicable global standards and regulations, such as ICH-GCP, IVDD/IVDR, MDR, FDA, and NMPA. Inclusion & Collaboration: Ability to partner effectively across diverse regions, cultures, and time zones to foster an environment of belonging and collaboration. Travel: Willingness to travel up to 25% depending on project phases. Who You Are : You are an analytical, strategic thinker who thrives in a fast-paced, matrixed environment. You are passionate about customer and patient-centricity, and you excel at integrating multiple cross-functional perspectives into a unified clinical strategy. Referenz Nr.: 925235 Rolle: Clinical Development Lead- Cardiovascular Industrie: Pharma Arbeitsort: Spain/Austria/UK Pensum: 100% Start Datum: ASAP Dauer: 12++ Months with a possibility of extension Bewerbungsfrist: 22/09/2026 attraktives Payroll-Only-Programm: +41 41 760 77 01.

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