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 modality
Private Health Insurance
Training bonus and Udemy access
23 vacation days per year
Christmas week off
Competitive salary and versátil compensation
ResponsabilidadesSupport 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 *, 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 principalesBachelor'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 * 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 * and MDR familiarity (nice to have)

📌 Clinical Operations Coordinator (España)
🏢 Inbrain Neuroelectronics
📍 España