Senior Clinical Research Coordinator

The University of Texas Rio Grande Valley; McAllen (TX); On-site; USD 65,000 - 90,000; Full time

Job summary

University of Texas Rio Grande Valley in Texas is seeking a Clinical Research Coordinator III to manage clinical projects, coordinate data collection, and ensure regulatory compliance. The role supports Principal Investigators and oversees study documentation, quality control, and patient safety in a hospital-research setting.

You will recruit participants, monitor enrollment, prepare IRB submissions, and collaborate with sponsors.

Qualifications

• Excellent communication skills and attention to detail.
• Ability to work in a highly matrixed environment with multiple departments.
• Extensive knowledge of best clinical research practices, techniques and standards.

Responsibilities

• Ensures accurate source documentation and forms per protocol.
• Identifies and recruits clinical research subjects and monitors enrollment goals.
• Submits IRB and regulatory documents to obtain approvals; drafts sponsor communications.
• Plans and reviews goals and requirements of new protocols and coordinates initiation.
• Develops education materials and training for patients and staff.

Skills

Communication

Attention to detail

Regulatory knowledge

Education

Bachelor7s degree

Job description

University of Texas Rio Grande Valley in Texas is seeking a Clinical Research Coordinator III to manage clinical projects, coordinate data collection, and ensure regulatory compliance. The role supports Principal Investigators and oversees study documentation, quality control, and patient safety in a hospital-research setting.

You will recruit participants, monitor enrollment, prepare IRB submissions, and collaborate with sponsors.