Traveling Clinical Research Associate

Texas Counseling Association; Houston (TX); On-site; USD 70,000 - 110,000; Full time

Benefits offered by this job

Health benefits

Competitive salary

Retirement plan

Life insurance

Wellbeing resources

Career development

Job summary

ICON, a global healthcare intelligence and clinical research organization, seeks a Clinical Research Associate in Houston. The role focuses on site visits, data integrity, and collaboration with investigators to drive high‑quality trial conduct.

You will travel about 60% and support protocol adherence, safety reporting, and regulatory compliance while contributing to study documentation and site management. Join ICON to advance clinical research and patient outcomes.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare field.
• Extensive experience as a Clinical Research Associate with regulatory knowledge.
• Ability to manage multiple sites and projects with strong organizational skills.
• Proficiency in monitoring, data integrity, and site management with clinical software.

Responsibilities

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

Skills

Clinical monitoring

Data integrity

Site management

Stakeholder management

Regulatory knowledge

Travel willingness

Education

Bachelor's degree in a relevant field

Tools

CTMS

Job description

ICON, a global healthcare intelligence and clinical research organization, seeks a Clinical Research Associate in Houston. The role focuses on site visits, data integrity, and collaboration with investigators to drive high‑quality trial conduct.

You will travel about 60% and support protocol adherence, safety reporting, and regulatory compliance while contributing to study documentation and site management. Join ICON to advance clinical research and patient outcomes.