CLINICAL AFFAIRS ASSOCIATE

Description

**At LVDBiotech (iVascular)**, we are a *Medical Devices* company located in Sant Vicenç dels Horts. We specialize in the development, manufacturing, and commercialization of advanced medical devices for the treatment of cardio-, neuro-, and endovascular diseases. Our focus is on delivering minimally invasive solutions that truly improve patients’ quality of life and establishing ourselves as a vascular reference by enhancing the value of technology and innovation. To achieve this, we internally control the entire process: from research and development to production, sterilization, and distribution. We call this Vertical Integration, enabling us to guarantee maximum quality, continuous innovation, and great agility to adapt to market needs. We are a national company in a growth and international expansion phase, with subsidiaries already established in Europe, the Americas, and Asia. Our purpose is very clear: to develop technologies that save and improve lives. **Position:** ----------- We are seeking a **CLINICAL AFFAIRS ASSOCIATE** to join our Clinical team at our facilities located in **Sant Vicenç dels Horts (Barcelona).** Your primary objective will be to provide support aimed at ensuring product safety and efficacy through clinical evaluation and post-market surveillance. **FUNCTIONS AND RESPONSIBILITIES:** * Clinical trial management * Selection and supervision of CROs and PIs * Selection of study sites and countries * Budgeting * Clinical documentation * Site\-iV contracts * Submissions to Ethics Committees / Regulatory Agencies * Recruitment * Results * Competitor analysis. * Management and preparation of scientific articles and congress abstracts. * Scientific literature review and bibliographic management software handling. * Support in coordinating and preparing Clinical Evaluation Plans (CEPs) and Clinical Development Plans (CDPs). * Support in coordinating and preparing Post-Market Clinical Follow-up (PMCF) Reports and Plans. * Support for Marketing and Commercial Departments. * Support in meetings with KOLs and investigators. **Requirements:** --------------- * Bachelor’s degree in Health Sciences, Biotechnology, Biomedicine, or related fields * Master’s degree in Clinical Trial Monitoring or similar * Minimum 2 years’ experience in similar roles. * Languages: Advanced English and Spanish proficiency. (A technical test will be administered.) **Additional Information:** --------------------- **WHAT WE OFFER** * Indefinite-term and stable contract within a globally impactful project currently undergoing international expansion. * Professional and personal development in a young and dynamic environment. * Competitive salary based on experience and an attractive benefits package. * Flexible working hours to support work-life/family balance. * Flexible compensation (restaurant vouchers, transportation, and childcare vouchers). * Access to the iWellness program: gym and physiotherapist available onsite. * Corporate events and gifts. * Company-subsidized cafeteria.