Remote CRA II: Clinical Trial Monitoring & Data

ICON Clinical Research; España; A distancia; EUR 35.000 - 50.000; Jornada completa

Descripción de la vacante

ICON Strategic Solutions is seeking a Clinical Research Associate II to work from home-based in Barcelona. You will design and analyze clinical trials, monitor sites, and ensure data integrity while contributing to innovative treatments and therapies.

Responsibilities include site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance and patient safety, and collaborating with investigators. Travel about 60% to sites 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

• Contribute to clinical trial monitoring activities and deliverables.
• Conduct site qualification, initiation, monitoring, and close-out visits.
• Ensure protocol compliance, data integrity, and patient safety.
• Collaborate with investigators and site staff to facilitate study conduct.
• Perform data review and resolution of queries for high-quality data.
• Assist in preparation and review of study documentation, including protocols and clinical study reports

Conocimientos

Site monitoring

Data review

Regulatory knowledge

Communication

Educación

Bachelor's degree in scientific or healthcare field

Descripción del empleo

ICON Strategic Solutions is seeking a Clinical Research Associate II to work from home-based in Barcelona. You will design and analyze clinical trials, monitor sites, and ensure data integrity while contributing to innovative treatments and therapies.

Responsibilities include site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance and patient safety, and collaborating with investigators. Travel about 60% to sites is required.