Remoto: Trabajo híbrido

OverviewIn this role, you support the planning, coordination, and execution of clinical investigations sponsored by INBRAIN. You work with internal teams, CROs, vendors, and investigational sites to ensure studies run efficiently, compliantly, and on schedule. You will help bring advanced healthcare solutions to market and contribute to improving patients' lives. The role offers exposure to cutting-edge neurotechnology and a collaborative, growth-oriented culture. You will have a meaningful impact by enabling high-quality clinical operations and continuous process improvement.Compensaciones / BeneficiosHybrid working modalityPrivate Health InsuranceTraining bonus and Udemy access23 vacation days per yearChristmas week offCompetitive salary and adaptable compensationResponsabilidadesSupport planning and coordination of clinical investigations and investigator-initiated studiesAssist with study start-up, study tracking, and operational activitiesCoordinate interactions with CROs, vendors, and investigational sitesManage and maintain study documentation and Trial Master Files (TMF)Contribute to compliance with ICH-GCP, ISO 14155, MDR,



and internal proceduresSupport clinical data review and data quality activities with CRO as applicablePrepare study status updates, reports, and operational metricsContribute to development and continuous improvement of clinical SOPs and processesRequisitos principalesBachelor's degree in Life Sciences, Biomedical Engineering, or related field+2 years of experience in clinical research, trial coordination, data management, or related roleUnderstanding of clinical research processes and ICH-GCPExcellent written and verbal communication skills in EnglishStrong organisational and coordination skillsAbility to manage multiple priorities and deadlines with attention to detailEffective communication and stakeholder managementProactive, collaborative, and adaptable approachExposure to Clinical Data Management or EDC systems (nice to have)Experience in medical device clinical research (nice to have)Familiarity with ISO 14155 and MDR requirements (nice to have)Experience working with CROs, vendors, and investigational sites (nice to have)excellent written and verbal communicationstrong organizational skillsproactive and collaborativeICH-GCP knowledgeClinical Data Management or EDC systems (nice to have)ISO 14155 and MDR familiarity (nice to have)

📌 Clinical Operations Coordinator (Barcelona)
🏢 Jobrapido
📍 Barcelona