VHIR – Clinical Research Technician
Act as the primary liaison between all participating clinical centres, providing support to clinicians and ensuring consistent communication regarding study timelines, procedures and requirements
Identify and resolve protocol deviations in collaboration with clinical teams.
Oversee accurate and timely data collection from each centre, ensuring data integrity, consistency and completeness before database lock.
Perform preliminary data analysis
Generate interim reports, metrics and summaries for internal review.
Conduct routine monitoring visits (remote or on-site) to ensure quality and compliance.
Support safety reporting processes (SAEs/AEs), ensuring correct documentation and follow-up.
Help solve practical issues related to logistics, sample handling, study workflows or documentation.
Assist with the coordination of study materials, devices or investigational products.
Maintain accurate documentation of study activities, communications and deviations.
Assist in the preparation of final clinical study reports.
Provide feedback from clinical sites to internal teams to support product evaluation and improvement.
📌 Tipus d’oferta: Contracte de tècnic
👤 Perfil buscat:
Bachelor’s degree in Science
Fluency in Catalan, Spanish and English (business level)
High level of autonomy and responsibility with experience working in a multidisciplinary team
Strong organisational and communication skills
Data analysis and interpretation
Advanced Excel skills