Senior Clinical Research Coordinator Interventional Trials

Revival Research Institute, LLC; Denton (TX); On-site; USD 60,000 - 80,000; Full time

Job summary

Revival Research Institute, LLC is seeking an experienced Clinical Research Coordinator to independently manage industry-sponsored interventional trials at our Denton site. You will own studies from initiation to close-out, coordinate visits, enroll participants, and ensure regulatory compliance while collaborating with investigators and staff.

Responsibilities include screening, data management, regulatory duties, IP accountability, and sponsor/IRB communications.

Qualifications

• 2+ years as a Clinical Research Coordinator at a research site.
•  
• Demonstrated experience independently obtaining informed consent on interventional protocols.
• Hands-on experience with EDC platforms.
• Demonstrated experience hosting monitoring visits and resolving monitoring findings independently.
• Working knowledge of ICH-GCP E6(R3) and 21 CFR Parts 11, 50, 54, 56, and 312, and HIPAA.
• Current phlebotomy competency, as well as IV certification, is preferred.
• Proficiency in Microsoft Office and excellent verbal and written communication.
• Ability to work on-site in Denton, Texas.

Responsibilities

• Screening, recruitment, and enrollment following protocol.
• Data collection, entry into EDC, and coordinating monitoring visits.
• Regulatory document management and ensuring inspection-ready files.
• Sponsor and IRB communication and timely regulatory reporting.
• Investigational product accountability and handling.
• Maintain up-to-date knowledge of ICH-GCP and FDA regulations.

Skills

Strong communication

Independent ownership

Data management

Regulatory knowledge

Microsoft Office

Ability to work on-site

Quality assurance

Team coordination

Education

Master's degree in health-related field

Tools

EDC platforms

Microsoft Office

Job description

Revival Research Institute, LLC is seeking an experienced Clinical Research Coordinator to independently manage industry-sponsored interventional trials at our Denton site. You will own studies from initiation to close-out, coordinate visits, enroll participants, and ensure regulatory compliance while collaborating with investigators and staff.

Responsibilities include screening, data management, regulatory duties, IP accountability, and sponsor/IRB communications.