Clinical Research Associate II – Monitoring & Data

ICON San Antonio; Madrid; On-site; EUR 42,000 - 56,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning options

Global support network

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II in Madrid to monitor trials, manage study quality, and ensure patient safety. You will work within a sponsor-dedicated model, applying rigorous data review and regulatory knowledge.

You will qualify sites, coordinate with investigators, and contribute to study documentation while traveling up to roughly 60% of your time. A scientific or healthcare background and CRA experience are required.

Qualifications

• 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%).

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.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Skills

Clinical trial monitoring

Communication skills

Organizational skills

Independent work

Travel willingness

Education

Bachelor's degree in science/healthcare

2+ years CRA experience

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II in Madrid to monitor trials, manage study quality, and ensure patient safety. You will work within a sponsor-dedicated model, applying rigorous data review and regulatory knowledge.

You will qualify sites, coordinate with investigators, and contribute to study documentation while traveling up to roughly 60% of your time. A scientific or healthcare background and CRA experience are required.