Clinical Research Associate

Real; Dallas (TX); On-site; USD 80,000 - 120,000; Full time

Job summary

Real is seeking a Clinical Monitoring Specialist to monitor trial sites, ensure patient safety and protocol compliance, and maintain high-quality data collection. You will conduct site visits, review documentation, and ensure GCP/regulatory adherence while supporting recruitment and retention efforts.

The role requires travel around 60% and close collaboration with investigators, coordinators, IRBs, vendors, and internal teams to resolve issues and keep studies on track.

Qualifications

• Experience working on complex protocols.
• End-to-end site monitoring experience.
• Experience tracking timelines.
• Site report writing experience.

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.

Skills

Complex protocols

Site monitoring

Timeline tracking

Site report writing

Travel 60%

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.

Desired Skills and Experience

• Experience working on complex protocols
• End-to-end site monitoring experience
• Experience tracking timelines
• Site report writing experience
• Ability to travel ~60%

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