Clinical Evaluation Internship
hace 1 semana
AtiVascular , we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment ofcardio,neuro, andendovasculardiseases and to become a reference in the vascular field by enhancing the value of technology and innovation. We 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. We are currently seeking a passionate and experiencedClinical Evaluation Internship to join ourClinical team at our site inSant Vicenç dels Horts(Barcelona). This internship is a unique opportunity to gain hands-on experience in the clinical and regulatory field of medical devices, supporting the development of documentation required under the European Medical Device Regulation (MDR). You will work closely with experienced professionals, contributing to literature reviews and clinical analysis that directly impact the safety and performance evaluation of our products. KEY RESPONSIBILITIES: Support the development ofsystematic and documented literature reviews, using scientific and medical databases to contribute to Clinical Evaluation, PMCF activities, State of the Art assessment, protocol development, and any required ad hoc analyses. Analyze available clinical evidence (internal manufacturer data and published scientific literature) to evaluate devicesafety and performance. Assist in the preparation and generation ofLiterature Search ReportsandClinical Evaluation Reports (CERs). DESIRED PROFILE: High level of English and Spanish (minimum B2). Graduate inBiomedicine, Biotechnology, Biomedical Engineering, Pharmacy, or other Health Sciences–related fields. AMaster's degreerelated to the Pharmaceutical Industry or Clinical Trialswill be considered an asset. Strong interest in theclinical and regulatory field of medical devices. Good command oftechnical English(minimum B2), especially in scientific reading and writing. Basic knowledge ofscientific methodology, clinical trials, or systematic reviews (desirable). Proficiency or familiarity withscientific databases(e.g., PubMed) and reference management tools likeZoteroorMendeley(valuable). WHAT WE OFFER: Permanent and stable contract in a project with high global impact and expanding internationally. Professional and personal development in a vibrant, dynamic, and youthful environment. Competitive salary tailored to your experience, along with an attractive benefits package. Flexible working hours to support a healthy work-life balance. Flexible compensation (meal vouchers, transportation, and childcare assistance). Access to our iWellness program: gym and physiotherapist on site. Corporate events and gifts. Subsidized on-site company cafeteria.
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