CRA II: Clinical Trial Monitor & Data Integrity

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

Benefits offered by this job

Health and wellbeing programmes incl.

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes andWell

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II to design and analyse clinical trials in a sponsor-dedicated model. You will monitor trials, ensure data integrity, and collaborate with investigators to advance therapies.

You will travel approximately 60% and work in a fast-paced environment, contributing to study documentation and regulatory compliance. Employment requires legal work status in the country.

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 travel 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

Data review

ICH-GCP knowledge

Regulatory knowledge

Communication

Independent work

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 to design and analyse clinical trials in a sponsor-dedicated model. You will monitor trials, ensure data integrity, and collaborate with investigators to advance therapies.

You will travel approximately 60% and work in a fast-paced environment, contributing to study documentation and regulatory compliance. Employment requires legal work status in the country.