Clinical Research Associate Ii - Icon Clinical Plc

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

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.

• Annual leave entitlements
• Health insurance offerings
• Retirement planning offerings
• Global Employee Assistance Programme (TELUS Health)
• Life assurance
• Flexible country-specific benefits
• 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 dataContribute to preparation and review of study documentation, including protocols and clinical study reports
• 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
• Independent and collaborative work style
• Knowledge of clinical trial processes and ICH-GCP guidelines
• Data review and query resolution

Clinical Research Associate II - Icon Clinical PLC barcelona, catalunya, es