At iVascular, we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio, neuro, and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation.
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brWe 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.
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brWe are currently seeking a passionate and experienced Clinical Evaluation Specialist to join our Clinical team at our site in Sant Vicenç dels Horts (Barcelona).
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brYou will be responsible for the development a creation of Clinical Documents in accordance the European Medical Device Regulation conducting literature reviews and writing Clinical Evaluation Reports.
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brExecute comprehensive systematic literature reviews, ensuring robust methodology, full traceability and appropriate use of specialized scientific databases.
brCritically appraise clinical evidence (manufacturer-held data and published literature) to support conclusions on device safety and performance in accordance with EU MDR.
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brSupport the clinical evaluation strategy across the medical device portfolio, in close collaboration with Regulatory Affairs and Quality teams.
brMinimum of 3 years of hands-on experience in Clinical Evaluation of medical devices under EU MDR 2017/745.
brStrong expertise in scientific writing, literature appraisal and systematic literature searches.
brFluent English and Spanish (written and spoken).
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brPermanent and stable contract in a project with high global impact and expanding internationally.
brProfessional and personal development in a vibrant, dynamic, and youthful environment.
brHybrid working model with telework days, and flexible hours. From Monday to Thursday, start between 7:00 and 9:00 a.m.