CRA II: Lead Site Monitoring & Data Integrity

ICON Strategic Solutions; United States; Vor Ort; USD 70.000 - 90.000; Vollzeit

Benefits dieser Stelle

Annual leave

Health insurance

Retirement plan

LifeWorks EAP

Life assurance

Flexible country-specific benefits

Zusammenfassung

ICON Strategic Solutions is seeking a Clinical Research Associate II to design and analyse clinical trials and interpret complex medical data for sponsor-dedicated studies. You will monitor sites and ensure data integrity while contributing to study documentation and regulatory compliance.

The role requires 2+ years as a CRA, a scientific/healthcare degree, and willingness to travel up to about 60%. ICON emphasizes global expertise, career development, and a collaborative culture across sponsor

Qualifikationen

• 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 work independently and collaboratively in a fast-paced environment.
• Willingness to travel as required (approximately 60%).

Aufgaben

• 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

Kenntnisse

Clinical trial monitoring

ICH-GCP knowledge

Organizational skills

Communication skills

Travel willingness

Ausbildung

Bachelor's degree in a scientific or healthcare-related field

Jobbeschreibung

ICON Strategic Solutions is seeking a Clinical Research Associate II to design and analyse clinical trials and interpret complex medical data for sponsor-dedicated studies. You will monitor sites and ensure data integrity while contributing to study documentation and regulatory compliance.

The role requires 2+ years as a CRA, a scientific/healthcare degree, and willingness to travel up to about 60%. ICON emphasizes global expertise, career development, and a collaborative culture across sponsor