CRA II: Design & Monitor Clinical Trials (60% Travel)

KCR Placement; Madrid; On-site; EUR 42,000 - 56,000; Full time

Benefits offered by this job

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible country-specific optional ben

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II to join a sponsor-dedicated model and contribute to the development of treatments that benefit patients worldwide.

You will design and monitor clinical trials, interpret complex medical data, and collaborate with investigators to ensure data quality, patient safety, and regulatory compliance.

Travel is approximately 60% and you will work with ICON's global operations team to deliver high-quality study results.

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

Organizational skills

Communication skills

Team collaboration

Independent work

Travel willingness

Education

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

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II to join a sponsor-dedicated model and contribute to the development of treatments that benefit patients worldwide.

You will design and monitor clinical trials, interpret complex medical data, and collaborate with investigators to ensure data quality, patient safety, and regulatory compliance.

Travel is approximately 60% and you will work with ICON's global operations team to deliver high-quality study results.