PAt strongemiVascular /em /strong, we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of strongcardio /strong, strongneuro /strong, and strongendovascular /strongdiseases and to become a reference in the vascular field by enhancing the value of technology and innovation. /ppbr/ppWe are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration. /ppbr/ppWe are currently seeking a passionate and experienced strongemHead of Clinical Evaluation /em /strong to join our strongemClinical /em /strongteam at our site in strongSant Vicenç dels Horts /strong (Barcelona). /ppbr/ppstrongYou will be responsible for leading the Clinical Evaluation unit /strong, driving the company’s clinical strategy. You will oversee the development, writing and supervision of all key clinical documentation, ensuring high-quality systematic literature reviews and the preparation, review and approval of Clinical Evaluation Reports, always in full compliance with the European Medical Device Regulation. /ppbr/ppbr/ppstrongKEY RESPONSIBILITIES: /strong /pulliLead the strongClinical Evaluation unit /strong, managing the team and ensuring alignment with the company’s overall clinical strategy. /liliOversee and execute strongcomprehensive systematic literature reviews /strong, ensuring robust methodology, full traceability and the appropriate use of specialized databases. /liliCritically appraise all strongavailable clinical evidence /strong—both internal data and published literature—to support well-founded conclusions on device safety and performance. /liliDirect and contribute to the development, writing, validation and approval of strongLiterature Search Reports /strong and strongClinical Evaluation Reports (CERs) /strong. /liliPrepare key clinical documentation, including strongLiterature Search Reports, Clinical Evaluation Reports, PMCF Reports and SSCPs /strong. /li /ulpbr/ppstrongDESIRED PROFILE: /strong /pulliMedical degree (MD) is required, preferably (valuable) with specialization in cardiovascular, neurovascular or peripheral vascular medicine. /liliHigh level of English and Spanish. /lili10 years of experience with EU MDR 2017/745, including extensive authorship, review and approval of CERs and clinical documentation. /liliStrong experience authoring PMCF Reports, SSCPs, Clinical Evaluation Plans (CEP) and Clinical Evaluation Reports (CER). /liliValuable experience with ISO 14155 and other clinical investigation standards. /liliStrong expertise writing, literature appraisal and systematic literature searches. /liliFamiliarity with reference management tools (Zotero, Mendeley, etc.). /li /ulpbr/ppstrongWHAT WE OFFER: /strong /pulliPermanent and stable contract in a project with high global impact and expanding internationally. /liliProfessional and personal development in a vibrant, dynamic, and youthful environment. /liliCompetitive salary tailored to your experience, along with an attractive benefits package. /liliFlexible working hours to support a healthy work-life balance. /liliFlexible compensation (meal vouchers, transportation, and childcare assistance). /liliAccess to our iWellness program: gym and physiotherapist on site. /liliCorporate events and gifts. /liliSubsidized on-site company cafeteria. /li /ul