Remote CRA II — Spain-Based Clinical Trials Expert

Icon; Alcobendas; Presencial; EUR 42.000 - 65.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Retirement planning

Life assurance

Global Employee Assistance Programme

Annual leave

Descripción de la vacante

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re excited to invite a Clinical Research Associate II to join our team in Spain, working home-based with substantial travel requirements.

You will design and analyze clinical trials, monitor sites, ensure patient safety and data integrity, and contribute to study documentation. A strong background in CRA activities and ICH-GCP knowledge is required.

Formación

• 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 as required (approximately 60%)

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.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Conocimientos

Clinical trial monitoring

ICH-GCP knowledge

Organizational skills

Communication skills

Independent and collaborative work

Educación

Bachelor's degree

Descripción del empleo

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re excited to invite a Clinical Research Associate II to join our team in Spain, working home-based with substantial travel requirements.

You will design and analyze clinical trials, monitor sites, ensure patient safety and data integrity, and contribute to study documentation. A strong background in CRA activities and ICH-GCP knowledge is required.