Remote CRA II - Clinical Trials & Data Monitoring

Dowjones; Barcelona; Teletrabalho; EUR 42 000 - 65 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Annual leave

Health insurance

Retirement planning

Employee Assistance Programme (LifeWor

Life assurance

Flexible country-specific benefits

Resumo da oferta

ICON Strategic Solutions in Spain is seeking a Clinical Research Associate II to join a sponsor-dedicated model. The role involves monitoring visits, data review, and collaboration with investigators to ensure trial quality and patient safety.

The position offers a home-based setup in Spain with travel obligations around 60% of the time. You will design and analyze clinical trials, interpret complex medical data, and contribute to the advancement of innovative therapies.

Qualificações

• 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 travel as required (approximately 60%).

Responsabilidades

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring 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.

Conhecimentos

Organizational skills

Communication skills

Independence

Team collaboration

Attention to detail

Formação académica

Bachelor's degree in a scientific or healthcare field

Descrição da oferta de emprego

ICON Strategic Solutions in Spain is seeking a Clinical Research Associate II to join a sponsor-dedicated model. The role involves monitoring visits, data review, and collaboration with investigators to ensure trial quality and patient safety.

The position offers a home-based setup in Spain with travel obligations around 60% of the time. You will design and analyze clinical trials, interpret complex medical data, and contribute to the advancement of innovative therapies.