Remote CRA II — Clinical Trials Monitoring (Galicia)

ICON Clinical Research; España; Remote; EUR 36,000 - 60,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

LifeWorks support

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II to be home-based in Galicia. You will design and monitor clinical trials, interpreting complex data to support treatment development. The role emphasizes independence and collaboration with investigators, ensuring patient safety and data integrity.

You should have a scientific healthcare background and 3–4 years of CRA experience, with ICH-GCP knowledge and strong organizational skills. Willingness to travel approx.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum 3-4 years of experience as a Clinical Research Associate in CRO or Pharmaceutical Company.
• 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.

Responsibilities

• Contributing to clinical trial monitoring activities, delivering on your responsibilities.
• 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.

Skills

Clinical trial monitoring

ICH-GCP knowledge

Data review

Travel readiness

Independent and collaborative work

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II to be home-based in Galicia. You will design and monitor clinical trials, interpreting complex data to support treatment development. The role emphasizes independence and collaboration with investigators, ensuring patient safety and data integrity.

You should have a scientific healthcare background and 3–4 years of CRA experience, with ICH-GCP knowledge and strong organizational skills. Willingness to travel approx.