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 integral 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

📌 CRA II (Barcelona)
🏢 Icon Clinical
📍 Barcelona