Clinical Evaluation Internship

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. 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 experienced Clinical Evaluation Internship to join our Clinical team at our site in Sant 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 of systematic 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 device safety and performance. Assist in the preparation and generation of Literature Search Reports and Clinical Evaluation Reports (CERs). DESIRED PROFILE: High level of English and Spanish (minimum B2). Graduate in Biomedicine, Biotechnology, Biomedical Engineering, Pharmacy, or other Health Sciences–related fields. A Master's degree related to the Pharmaceutical Industry or Clinical Trials will be considered an asset. Strong interest in the clinical and regulatory field of medical devices. Good command of technical English (minimum B2), especially in scientific reading and writing. Basic knowledge of scientific methodology, clinical trials, or systematic reviews (desirable). Proficiency or familiarity with scientific databases (e.g., PubMed) and reference management tools like Zotero or Mendeley (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.