As a Clinical Research Associate II at ICON, you contribute to designing and analyzing clinical trials and interpreting medical data to advance innovative therapies. You will oversee site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance, data integrity, and patient safety. You will collaborate with investigators and site staff and support data review and study documentation. This role combines independent work with cross-functional teamwork to sustain trial quality and impact.
Compensaciones / Beneficios
- Annual leave entitlements
- Health insurance offerings
- Retirement planning offerings
- Integral Employee Assistance Programme (TELUS Health)
- Life assurance
- Flexible country-specific benefits
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 resolve 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
- Ability to travel at least 60% of the time (international and domestic) and a valid driver’s license
- Good level of English
- Strong organizational skills
- Effective communication
- Attention to detail
- Independent and collaborative work style
- Knowledge of clinical trial processes and ICH-GCP guidelines
- Data review and query resolution
📌 Clinical Research Associate II (Barcelona)
🏢 Icon Clinical
📍 Barcelona
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