Clinical Research Associate — Site & Data Quality Lead

Real Staffing Group; Texas; On-site; USD 68,000 - 90,000; Full time

Job summary

Real Staffing Group is seeking a Clinical Trial Monitor to oversee study sites in Wisconsin, United States. You will monitor patient safety, protocol compliance, and data quality across sites.

The role involves site visits, documentation review, and ensuring GCP compliance. You will train site staff and collaborate with investigators, IRBs, vendors, and internal teams to keep trials on track.

Responsibilities

• Monitor clinical trial sites to ensure patient safety, protocol compliance, and high-quality data collection.
• Conduct site visits, review study documentation, and maintain regulatory and GCP compliance.
• Support site performance, patient recruitment, and retention efforts.
• Partner with investigators, coordinators, IRBs, vendors, and internal teams to resolve issues and keep studies on track.
• Serve as the primary study contact for assigned sites, providing training, communication, and operational support throughout the trial.

Job description

• Role Overview:
• Monitor clinical trial sites to ensure patient safety, protocol compliance, and high-quality data collection.
• Conduct site visits, review study documentation, and maintain regulatory and GCP compliance.
• Support site performance, patient recruitment, and retention efforts.
• Partner with investigators, coordinators, IRBs, vendors, and internal teams to resolve issues and keep studies on track.
• Serve as the primary study contact for assigned sites, providing training, communication, and operational support throughout the trial.

EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

To find out more about Real, please visit www.realstaffing.com