OverviewAt Rieka Talent, we are currently looking for a Clinical Research Associate (CRA) to join an innovative and international company operating within the medical device industry.This position offers the opportunity to play a key role in clinical investigations, evidence generation, and regulatory documentation within a highly regulated and fast-growing environment.Position ObjectiveThe CRA will provide clinical and scientific expertise across clinical studies within a medical device environment. This role will be responsible for the clinical investigation lifecycle, including CRO coordination, clinical site identification, site feasibility, investigator engagement, clinical follow-up, and contribution to clinical documentation. The position is critical in ensuring quality, consistency, and regulatory readiness of clinical evidence, supporting informed decision-making and compliance throughout the medical device lifecycle.Key ResponsibilitiesClinical Studies: Design, plan, coordinate, and oversee clinical investigations for medical devices in compliance with EU MDR (2017/745), ISO 14155, and applicable regulationsIdentify and coordinate clinical investigation sites and investigatorsConduct feasibility assessments and maintain site follow-up activitiesAct as the main point of contact for CROs, investigators, and clinical sitesDraft clinical study protocols and essential clinical documentationCoordinate collection, review,



and consolidation of clinical data ensuring quality and traceabilityClinical DocumentationPreparation and maintenance of clinical sections of Technical Documentation, including:Clinical Evaluation Plan (CEP)Clinical Evaluation Report (CER)Clinical Development Plan (CDP)What the Company OffersHybrid working modelInternational and collaborative environmentOpportunity to join a growing and innovative companyExposure to global clinical projects within the medical device sectorHigh visibility and direct interaction with general teamsSalary: approximately €60,000 (B/a band, depending on experience and profile)What We Are Looking ForEducationUniversity degree in a health-related or biomedical field such as: Medicine, Pharmacy, Biomedical Sciences, Life Sciences, Nursing, or equivalentExperiencePrevious experience in clinical studies management, including: Study planning and initiationStudy oversight and coordinationClinical data review and reportingExperience within Clinical Development, Clinical Research, Medical Affairs, Regulatory Affairs, Medical Writing, or similar scientific rolesPrevious CRA experience and/or CRA qualificationExperience in medical devices, aesthetics, or dermatology will be highly valuedLanguagesFluent English and Spanish (written and spoken)Another European language is considered a plus

📌 Clinical Research Associate (Cra) (Barcelona)
🏢 Tamarind Intelligence
📍 Barcelona