CRA II: Clinical Trials Monitoring & Data Integrity

ICON Clinical Research; Madrid; On-site; EUR 45,000 - 65,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Childcare vouchers & other benefits

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II in Madrid to support sponsor-dedicated trials with ICON’s global expertise. The role involves monitoring activities, data review, and collaboration with investigators to ensure high-quality study conduct.

You will bring at least 2 years of CRA experience, a solid understanding of ICH-GCP, and strong organizational and communication skills. Travel approximately 60% is required to perform site visits across sites.

Qualifications

• 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

ICH-GCP knowledge

Regulatory compliance

Data review

Communication skills

Travel readiness

Education

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

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II in Madrid to support sponsor-dedicated trials with ICON’s global expertise. The role involves monitoring activities, data review, and collaboration with investigators to ensure high-quality study conduct.

You will bring at least 2 years of CRA experience, a solid understanding of ICH-GCP, and strong organizational and communication skills. Travel approximately 60% is required to perform site visits across sites.