Clinical Research Associate II: Global Trials & Data

Icon Clinical Plc; Barcelona; Presencial; EUR 40.000 - 60.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme (

Life assurance

Flexible country-specific benefits

Descripción de la vacante

Icon Clinical PLC is seeking a Clinical Research Associate II in Barcelona to oversee site qualification, initiation, monitoring, and close-out visits for clinical trials. You will ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff to facilitate study conduct.

The role requires 2+ years in CRA, knowledge of ICH-GCP, and a strong ability to work independently in a fast-paced environment.

Formación

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• Knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills with attention to detail.
• Willingness to travel at least 60% (international and domestic) and hold a valid driver’s license.
• Good level of English.
• Ability to work independently and collaboratively in a fast-paced environment.

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.

Conocimientos

Organizational skills

Communication skills

Attention to detail

Independent worker

Team collaboration

English proficiency

Educación

Bachelor's degree in a scientific/healthcare field

Descripción del empleo

Icon Clinical PLC is seeking a Clinical Research Associate II in Barcelona to oversee site qualification, initiation, monitoring, and close-out visits for clinical trials. You will ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff to facilitate study conduct.

The role requires 2+ years in CRA, knowledge of ICH-GCP, and a strong ability to work independently in a fast-paced environment.