Clinical Operations Coordinator (Medtech)

Location: Barcelona, Spain; hybrid working modality

Company

hirify.global develops graphene-based high-resolution neural systems for real-time precision neurology and brain-related disorders.

What you will do

• Support the planning and coordination of clinical investigations and investigator-initiated studies.
• Assist with study start-up, study tracking, and operational execution.
• Coordinate activities with CROs, vendors, and investigational sites.
• Maintain study documentation and Trial Master Files.
• Support clinical data review, data quality activities, status reporting, and operational metrics.
• Contribute to clinical SOP development and continuous improvement of operational processes.

Requirements

• Bachelor’s degree in Life Sciences, Biomedical Engineering, or a related field.
• At least 2 years of experience in clinical research, clinical trial coordination, data management, or a related role.
• Experience with Clinical Data Management or EDC systems.
• Understanding of clinical research processes and ICH-GCP principles.
• Excellent written and verbal English communication skills; applications must be submitted in English.
• Strong organisation, coordination, stakeholder management, prioritisation, and attention-to-detail skills.

Nice to have

• Experience in medical device clinical research.
• Familiarity with ISO 14155 and MDR requirements.
• Experience working with CROs, vendors, and investigational sites.

Culture & Benefits

• Collaborative environment focused on open communication, knowledge sharing, mutual respect, and innovation.
• Exposure to cutting-edge healthcare technologies and innovative solutions.
• Private health insurance and an internal flexible compensation scheme.
• Training bonus, professional development opportunities, and access to Udemy.
• 23 vacation days per year and Christmas week off.
• Competitive salary based on experience and skills.