Clinical Lead

Description

**LVD Biotech \- iVascular Group** is an international medical technology group specializing in the development, manufacturing, marketing, and distribution of innovative medical devices for the treatment of vascular system disorders worldwide. Our vertically integrated business model enables us to manage the entire product lifecycle. The group comprises two highly specialized and complementary companies: * LVD Biotech, our innovation hub, leads and drives research and development of new technologies, managing the full product development cycle—from initial concept generation through to regulatory dossier preparation—including knowledge generation and protection via intellectual property. * iVascular transforms this innovation into medical solutions delivered to healthcare professionals and patients through manufacturing, logistics, marketing, and international commercialization of a portfolio of medical devices for Coronary, Peripheral, and Neurovascular applications. With a team of over 600 professionals and commercial presence in more than 86 countries, both companies operate in close integration within a continuously collaborative environment that combines science, innovation, industrial excellence, and the highest quality standards. Together, we drive the development of cutting-edge medical solutions with a shared goal: improving patients’ quality of life worldwide. **Position:** ----------- We are seeking a **CLINICAL LEAD** to join our Clinical team at our facilities located in **Sant Vicenç dels Horts (Barcelona).** Your primary objective will be to ensure product safety and efficacy through clinical evaluation and post-market surveillance. **KEY RESPONSIBILITIES:** 1\- Coordination, Management, and Planning of Clinical Investigations: * Selection and supervision of CROs and Principal Investigators (PIs) * Selection of clinical sites and countries * Budgeting * Clinical documentation * Site-iVascular contracts * Submissions to Ethics Committees / Regulatory Agencies * Patient recruitment * Results analysis 2\- Interaction with Key Opinion Leaders (KOLs) 3\- Leading meetings with KOLs, investigators, and CROs 4\- Competitive analysis 5\- Scientific publications and conference abstracts: management and preparation 6\- Preparation of Clinical Evaluation Plans (CEPs) and Clinical Development Plans (CDPs) 7\- Preparation of Post-Market Clinical Follow-up (PMCF) reports and plans 8\- Preparation of Summary of Safety and Clinical Performance (SSCP) reports 9\- Scientific literature review and bibliographic management 10\- Cross-functional collaboration with Marketing and Commercial departments **Requirements:** --------------- **IDEAL PROFILE:** * Bachelor’s degree in Health Sciences, Biotechnology, Biomedicine, or related fields. A PhD is advantageous. * Minimum 3 years of experience in clinical investigations. * Languages: Advanced English and Spanish proficiency (technical assessment required). **Additional Information:** --------------------- **WHAT WE OFFER** * Permanent, stable employment within a high-impact global project undergoing active international expansion. * Professional and personal development in a young, dynamic environment. * Competitive salary commensurate with experience, plus an attractive benefits package. * Flexible working hours to support work-life balance. * Flexible compensation (meal vouchers, transportation allowances, childcare support). * Access to the iWellness program: on-site gym and physiotherapy services. * Corporate events and gifts. * Company-subsidized cafeteria. Benefit: Health insurance, Flexible working hours, Remote work, On-the-job training, Language courses, Mental health support, Wellness program, Company cafeteria, Free gym at offices, Subsidized meals