Overview In this role, you will design and analyse clinical trials and monitor sites to ensure data quality and patient safety. You will work with investigators and site staff to keep studies on track and compliant with protocols and ICH-GCP. You contribute to study documentation and data review while operating in a fast-paced, collaborative environment.

You will travel up to ~60% to support general trial activities and deliver quality trial outcomes. Compensaciones / Beneficios Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Responsabilidades Conduct site qualification, initiation, monitoring, and close-out visits Ensure protocol compliance, data integrity,



and patient safety Collaborate with investigators and site staff to facilitate study conduct Perform data review and resolve queries to maintain high-quality clinical data Contribute to preparation and review of study documentation (protocols, CSRs) Requisitos principales Bachelor in Science or Healthcare-related field Minimum 2 years of Clinical Research Associate experience In-depth knowledge of clinical trial processes, regulations, and ICH-GCP Strong organizational and communication skills with attention to detail Ability to work independently and collaboratively in a fast-paced environment Willingness to travel ~60% strong organizational skills effective communication attention to detail clinical trial processes ICH-GCP guidelines data review and query resolution

📌 Clinical Research Assistant (Barcelona)
🏢 Icon Clinical
📍 Barcelona