CRA II: Clinical Trial Monitoring & Data Quality

ICON Strategic Solutions; Lisboa; On-site; EUR 40,000 - 60,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II in Lisbon, Portugal. You will design and monitor clinical trials, interpreting medical data to advance treatments that benefit patients worldwide.

You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring protocol adherence, data integrity, and patient safety. Travel up to ~60% is 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.

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

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II in Lisbon, Portugal. You will design and monitor clinical trials, interpreting medical data to advance treatments that benefit patients worldwide.

You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring protocol adherence, data integrity, and patient safety. Travel up to ~60% is required.