Clinical Research Associate — Travel‑Heavy, Global Trials

ICON Strategic Solutions; Chicago (IL); On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

Competitive base salary

Health and wellbeing programs

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programs

Learning and development opportunities

Job summary

ICON Strategic Solutions seeks a Clinical Research Associate to design and analyze clinical trials, interpreting complex data and contributing to innovative therapies. You will monitor sites, ensure protocol and data integrity, and collaborate with investigators to support study conduct.

You will travel approximately 60% and work within a fast-paced, regulated environment, ensuring patient safety and high-quality data throughout the trial lifecycle.

Qualifications

• Bachelor's degree in a scientific field and clinical trial experience required.
• Extensive Clinical Research Associate experience with regulatory knowledge.
• Ability to manage multiple sites and projects with strong organizational skills.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits.
• Ensure protocol compliance, data integrity, and patient safety throughout trials.
• Collaborate with investigators and site staff to facilitate study conduct.
• Perform data review and resolve queries to maintain quality data.
• Contribute to study documentation like protocols and reports.

Skills

Clinical trial monitoring

Regulatory knowledge

Data integrity

Site management

Data analysis

Stakeholder management

Travel readiness

Education

Bachelor's degree in a relevant scientific discipline

Tools

CTMS

EDC

Job description

ICON Strategic Solutions seeks a Clinical Research Associate to design and analyze clinical trials, interpreting complex data and contributing to innovative therapies. You will monitor sites, ensure protocol and data integrity, and collaborate with investigators to support study conduct.

You will travel approximately 60% and work within a fast-paced, regulated environment, ensuring patient safety and high-quality data throughout the trial lifecycle.