Overview

In this CRA II role, you design and monitor clinical trials, ensuring data integrity and patient safety while supporting study teams. You’ll collaborate with investigators and staff to enable smooth study conduct and high-quality documentation. Your work helps advance innovative treatments by translating complex data into actionable insights. This position offers an opportunity to impact patients’ lives within a values‑driven, collaborative team.

Compensaciones / Ventajas

- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- 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 for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process




- Collaborate with investigators and site staff to facilitate smooth study conduct
- Perform data review and resolution of queries to maintain high-quality clinical data
- Contribute to preparation and review of study documentation, including protocols and clinical study reports

Requisitos principales

- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills, with attention to detail
- Ability to work independently and collaboratively in a fast-paced environment
- Willingness to travel approximately 60%

- Strong communication skills
- Attention to detail
- Collaborative mindset
- Clinical trial monitoring
- Data review and query resolution
- ICH-GCP knowledge

📌 CRA 2 o SCRA (Barcelona)
🏢 Icon Clinical
📍 Barcelona