Global CRA II - Drive Clinical Trials & Patient Impact

ICON Strategic Solutions; United States; Vor Ort; USD 65.000 - 95.000; Vollzeit

Benefits dieser Stelle

Annual leave

Health insurance

Retirement plan

Employee assistance program

Life insurance

Flexible benefits

Zusammenfassung

ICON Strategic Solutions, the sponsor-dedicated arm of ICON, is recruiting a Clinical Research Associate II to join a global FSP environment. You will design and monitor trials, interpret complex data, and contribute to therapies that benefit patients worldwide.

In this CRA II role, you will perform site qualification, initiation, monitoring and close-out visits, ensure data integrity and patient safety, and collaborate with investigators.

Qualifikationen

• Bachelor's degree in a scientific or healthcare field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes and ICH-GCP.
• Willingness to travel approximately 60%.

Aufgaben

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensure 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

Kenntnisse

CRA experience

ICH-GCP knowledge

Data review

Regulatory compliance

Travel readiness

Communication skills

Ausbildung

Bachelor's degree in science/healthcare

Jobbeschreibung

ICON Strategic Solutions, the sponsor-dedicated arm of ICON, is recruiting a Clinical Research Associate II to join a global FSP environment. You will design and monitor trials, interpret complex data, and contribute to therapies that benefit patients worldwide.

In this CRA II role, you will perform site qualification, initiation, monitoring and close-out visits, ensure data integrity and patient safety, and collaborate with investigators.