Clinical Trials Operations Coordinator

Inbrain Neuroelectronics; Bellprat; On-site; EUR 38,000 - 60,000; Full time

Benefits offered by this job

23 days annual holiday

Company Christmas break

Private health insurance

Udemy learning account

Annual training allowance

Job summary

Inbrain Neuroelectronics seeks a Clinical Research Coordinator to support planning, start-up, tracking, and operational activities for clinical investigations. You will collaborate with CROs, vendors, and investigational sites while maintaining TMF documentation and ensuring compliance with ICH-GCP and MDR requirements.

The role emphasizes data quality, study metrics, and SOP improvements, with English as the company culture language.

Qualifications

• Bachelor’s degree in Life Sciences or related field.
• +2 years in clinical research, coordination, data management, or related role.
• Experience in Clinical Data Management or EDC systems.
• Understanding of clinical research processes and ICH-GCP principles.
• Excellent written and verbal communication in English.

Responsibilities

• Coordinate 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 improvement of clinical SOPs and processes.

Skills

Clinical research

Data management

EDC systems

ICH-GCP

English fluency

Organization

Prioritization

Stakeholder mgmt

Education

Bachelor’s degree in life sciences/related

Job description

Inbrain Neuroelectronics seeks a Clinical Research Coordinator to support planning, start-up, tracking, and operational activities for clinical investigations. You will collaborate with CROs, vendors, and investigational sites while maintaining TMF documentation and ensuring compliance with ICH-GCP and MDR requirements.

The role emphasizes data quality, study metrics, and SOP improvements, with English as the company culture language.