Clinical Research Associate II – Trials Monitoring (Midwest)

ICON Strategic Solutions; Texas; On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

Health insurance

Retirement planning

Employee assistance program

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate to join a sponsor-dedicated model, backed by ICON’s global expertise. The CRA II will design and analyze trials, interpreting complex medical data to advance therapies that benefit patients worldwide.

Responsibilities include site qualification and monitoring visits, ensuring data integrity and patient safety, and collaborating with investigators.

Qualifications

• Bachelor's degree in 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.
• 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 smooth study conduct.
• Perform data review and resolution of queries to maintain high-quality clinical data.
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports.

Skills

Clinical trial monitoring

ICH-GCP knowledge

Strong communication

Travel readiness

Independent working

Education

Bachelor's degree in science/healthcare

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate to join a sponsor-dedicated model, backed by ICON’s global expertise. The CRA II will design and analyze trials, interpreting complex medical data to advance therapies that benefit patients worldwide.

Responsibilities include site qualification and monitoring visits, ensuring data integrity and patient safety, and collaborating with investigators.