Clinical Research Associate - PT Impact, 60% Travel

ICON Strategic Solutions; Houston (TX); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Health, dental, vision coverage

Retirement plans

Life insurance

Disability coverage

Employee assistance program

Career development opportunities

Job summary

ICON is seeking a Clinical Research Associate in Houston to monitor clinical trials and ensure patient safety and data integrity. Travel of about 50–60% is required, with responsibilities spanning site initiation, monitoring visits, data review, and collaboration with investigators.

The role requires a Bachelor’s degree in a scientific field and extensive CRA experience, with strong organizational and communication skills to manage multiple sites and projects effectively.

Qualifications

• Bachelor's degree in a relevant scientific or healthcare field.
• Extensive experience as a Clinical Research Associate with understanding of trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects with strong organizational skills.
• Expertise in monitoring practices, data integrity, and site management with relevant tools.

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 for smooth study conduct.
• Perform data review and resolve queries to maintain high-quality data.
• Assist in study documentation including protocols and study reports.

Skills

Clinical trial monitoring

Regulatory knowledge

Site management

Communication

Education

Bachelor's degree in a relevant scientific field

Tools

Clinical trial software

Data integrity tools

Job description

ICON is seeking a Clinical Research Associate in Houston to monitor clinical trials and ensure patient safety and data integrity. Travel of about 50–60% is required, with responsibilities spanning site initiation, monitoring visits, data review, and collaboration with investigators.

The role requires a Bachelor’s degree in a scientific field and extensive CRA experience, with strong organizational and communication skills to manage multiple sites and projects effectively.