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 adaptable 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 - Inbrain Neuroelectronics (Barcelona)
🏢 Inbrain Neuroelectronics
📍 Barcelona