Clinical Research and Regulatory Specialist | MedTechLocation: Spain (Remote)Employment type: Full-timeRole SummaryWe are looking for a motivated junior professional who wants to develop their career in the MedTech and IVD sector.As a Clinical Research and Regulatory Specialist, you will support clinical research activities, scientific and medical writing, and the creation of documentation essential to product validation and regulatory pathways.You will work closely with senior experts and multidisciplinary teams, gaining hands-on experience with clinical investigations, performance studies (ISO 14155 and ISO 20916), technical documentation, and clinical evidence development.Ideal for candidates with 0.5–2 years of experience in MedTech, IVD, clinical research or R&D — or strong scientific backgrounds eager to enter the industry.ResponsibilitiesYou will:Support the preparation and execution of Clinical Investigations and Performance StudiesAssist in developing study documentation (protocols, CRFs, ICFs)Collaborate with study sites and internal teams following ISO 14155 and ISO 20916 standardsHandle study documentation and communication with investigatorsAssist with monitoring‐support activities and data‐related tasksContribute to scientific and medical writing, including study summaries and evidence-based contentSupport literature reviews, background research, and documentation preparationAssist in drafting components of clinical evidence documentation under supervisionHelp coordinate project activities, timelines, and communicationYou will receive structured onboarding, mentoring,



and progressive responsibility.You are not expected to know everything on day one — you will learn with us.Requirements (Must‐Have)Based in Spain or eligible for a Spanish employment contract0.5–2 years of experience in MedTech, IVD, clinical research, or R&DStrong interest in MedTech, IVDs, clinical research, and scientific developmentBachelor's degree in Life SciencesEnrolment in or completion of a Master's degree in Life SciencesKnowledge of GCP and clinical/lab standardsAdvanced English (C1–C2), especially for scientific writingMotivation to grow in a dynamic and international environmentAvailability for remote work with occasional in‐person activitiesNice to HaveExposure to ISO 14155 or ISO 20916R&D experienceRegulatory exposureAcademic research experience or authorship in scientific literatureWhy Join MDx CROAt MDx CRO, you will join a dynamic and rapidly growing company recognised across the MedTech and IVD industry. We offer:Structured onboarding and continuous trainingClose mentorship from senior specialistsExposure to real clinical and scientific projectsGrowth opportunities as your skills developAbout MDx CROMDx CRO is a leading Contract Research Organisation specialising in in vitro diagnostics (IVDs) and medical devices. We provide regulatory consulting, clinical research, and quality assurance services, helping clients bring safe and effective products to market in full compliance with general regulatory standards.We operate on five core principles:Make it POSSIBLEMake it WIN-WINKeep IMPROVINGKeep GROWINGKeep it DIVERSEOur VisionTo democratise access to world-class regulatory and clinical strategies, ensuring safer and more effective medical technologies for all.Our MissionWe pioneer emerging technologies and navigate uncharted territories to redefine the future of the medical sector.Grow with UsIf you want to accelerate your development in the MedTech and IVD sector within a supportive and expert‐driven environment, we would love to hear from you.

📌 Clinical Research Specialist | Medtech (Huesca)
🏢 MDx CRO
📍 Huesca