Clinical Research Associate II — Trials & Data Quality

Regulatory Jobs; Chicago (IL); On-site; USD 91,000 - 114,000; Full time

Benefits offered by this job

Competitive base salary

Performance related incentives

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes

Learning and development opportunities

Career pathways

Job summary

ICON Strategic Solutions, a sponsor-dedicated unit within ICON, seeks a Clinical Research Associate II for the Central/Mid-West region. You will design and analyze trials and contribute to advancing treatments that benefit patients worldwide.

As a CRA II, you conduct site visits, ensure data quality, and collaborate with investigators to support study conduct. Travel ~60% and strong ICH-GCP knowledge are required.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of CRA experience.
• Knowledge of clinical trial processes and ICH-GCP guidelines.
• Strong organizational and communication skills.
• Ability to travel approximately 60%.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborate with investigators and site staff to facilitate smooth study conduct.
• Perform data review and resolution of queries to maintain high-quality clinical data.
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports.

Skills

Clinical monitoring

ICH-GCP knowledge

Data review

Regulatory compliance

Travel readiness

Education

Bachelor's degree in life sciences

Job description

ICON Strategic Solutions, a sponsor-dedicated unit within ICON, seeks a Clinical Research Associate II for the Central/Mid-West region. You will design and analyze trials and contribute to advancing treatments that benefit patients worldwide.

As a CRA II, you conduct site visits, ensure data quality, and collaborate with investigators to support study conduct. Travel ~60% and strong ICH-GCP knowledge are required.