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Clinical research associate (cra) (barcelona)

Barcelona
Novartis
Publicada el 9 junio
Descripción

Experteer Overview
As a Clinical Research Associate, you drive trial delivery by building trusted site partnerships and ensuring high-quality, compliant execution across Phase I–IV trials. You will monitor sites, identify risks, and work with cross-functional teams to deliver trials with integrity and impact. This role centers on patient safety, data quality, and continuous improvement in site performance. You will collaborate across functions to support recruitment challenges and study conduct, contributing to the company’s clinical innovation mission.

Compensaciones / Ventajas
• Serve as primary contact between Novartis and clinical trial sites to foster strong partnerships
• Manage assigned Phase I–IV study sites in line with protocols, monitoring plans and regulatory requirements
• Conduct site initiation visits to train site teams on study protocols and expectations
• Deliver ongoing training for amendments and new site personnel to maintain compliance
• Perform on-site and remote monitoring to ensure patient safety, data integrity, and protocol adherence
• Proactively assess site performance, identify risks, and implement mitigation strategies
• Identify process gaps and collaborate with sites to drive continuous improvement and operational excellence
• Promote a strong compliance culture with attention to ethics, regulations, and data privacy
• Build site relationships to improve patient recruitment and reduce operational challenges
• Lead site closeout activities with follow-up actions and proper documentation and archiving

Responsabilidades
• Bachelor’s degree in a scientific or healthcare-related discipline
• Minimum 1 year of experience in clinical research, including monitoring or site management
• Understanding of clinical trial processes, GCP and ICH guidelines
• Knowledge of regulatory requirements and standards (global and local authorities)
• Strong communication and relationship-building skills for site collaboration
• Ability to manage multiple priorities with strong organization and time management
• Analytical and risk-based thinking with ability to identify issues and implement mitigation strategies
• Fluency in written and spoken English and the local language

Requisitos principales
•

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