CRA II – Cardio & Obesity Trials (60% Travel)

KCR Placement; San Antonio (TX); On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

Health insurance

Retirement planning options

Global Employee Assistance Programme

Life assurance

Annual leave

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II based in the United States (San Antonio, TX) to support sponsor-dedicated cardio and obesity trials. You will monitor clinical sites, ensure data integrity, and collaborate with investigators to advance treatments that benefit patients worldwide.

You will review data, resolve queries, and help prepare study documentation. Travel up to 60% is required in a fast-paced, globally supported environment.

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 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

Independent work

Travel readiness

Education

Bachelor's degree in science/healthcare

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II based in the United States (San Antonio, TX) to support sponsor-dedicated cardio and obesity trials. You will monitor clinical sites, ensure data integrity, and collaborate with investigators to advance treatments that benefit patients worldwide.

You will review data, resolve queries, and help prepare study documentation. Travel up to 60% is required in a fast-paced, globally supported environment.