CRA II: Cardio & Obesity Trials Monitoring

ICON Strategic Solutions; Florida; On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Annual leave

Retirement planning

Employee assistance program

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II to monitor trials and ensure data integrity. The role requires traveling up to 60% and working in a sponsor-dedicated model to support cardio and obesity trials.

Located in the South, TX, with opportunities to contribute to study design and regulatory compliance. You will perform site visits, ensure patient safety, and collaborate with investigators to advance clinical research across multiple sites.

Qualifications

• Bachelor’s degree in a scientific or healthcare-related field or equivalent.
• Minimum of 2 years of experience as a Clinical Research Associate.
• Knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Willingness to travel approximately 60%.

Responsibilities

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

Skills

Clinical trial monitoring

Communication

Organization

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 monitor trials and ensure data integrity. The role requires traveling up to 60% and working in a sponsor-dedicated model to support cardio and obesity trials.

Located in the South, TX, with opportunities to contribute to study design and regulatory compliance. You will perform site visits, ensure patient safety, and collaborate with investigators to advance clinical research across multiple sites.