Overview In 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 / Beneficios Hybrid working modality Private Health Insurance Training bonus and Udemy access 23 vacation days per year Christmas week off Competitive salary and versátil compensation Responsabilidades Support planning and coordination of clinical investigations and investigator-initiated studies Assist with study start-up, study tracking, and operational activities Coordinate interactions with CROs, vendors, and investigational sites Manage and maintain study documentation and Trial Master Files (TMF) Contribute to compliance with ICH-GCP, ISO 14155, MDR, and internal procedures Support clinical data review and data quality activities with CRO as applicable Prepare study status updates,



reports, and operational metrics Contribute to development and continuous improvement of clinical SOPs and processes Requisitos principales Bachelor’s degree in Life Sciences, Biomedical Engineering, or related field +2 years of experience in clinical research, trial coordination, data management, or related role Understanding of clinical research processes and ICH-GCP Excellent written and verbal communication skills in English Strong organisational and coordination skills Ability to manage multiple priorities and deadlines with attention to detail Effective communication and stakeholder management Proactive, collaborative, and adaptable approach Exposure 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 communication strong organizational skills proactive and collaborative ICH-GCP knowledge Clinical Data Management or EDC systems (nice to have) ISO 14155 and MDR familiarity (nice to have)

📌 Clinical Operations Coordinator (Barcelona)
🏢 Jobrapido
📍 Barcelona