Infusion RN - Lubbock, TX - Per Diem

The role

A Clinical Research Coordinator I – RN manages industry-sponsored clinical trials. This role involves managing patient interactions, ensuring protocol compliance, and maintaining data integrity.

What you will do

• Administratively and clinically manage industry-sponsored clinical trials.
• Schedule all patient research visits and procedures.
• Enter study and subject-specific information into the CTMS.
• Complete and maintain study documentation including consent forms and case report forms.
• Schedule and prepare for monitor visits.
• Maintain inventory of study equipment and supplies.
• Lead patient recruitment activities.
• Conduct patient visits as outlined within each study protocol.
• Dispense study medication, collect vital signs, and perform ECGs.
• Perform blood draws and process and ship specimens.

Required qualifications

• Active Registered Nurse (RN) license
• Solid nursing background with a concentration in, or willingness to develop advanced knowledge of, GI specialty
• Ability to execute research tasks with guidance from experienced staff, PIs, and management
• Strong written and verbal communication skills
• Ability to read, interpret, and apply clinic policies and research protocols
• Proficiency in standard office software and CTMS platforms
• Highly organized with the ability to manage multiple priorities and meet deadlines
• Ability to work independently and collaboratively in a fast-paced environment

Nice to have

• 1–2 years of clinical research experience
• Prior GI or hepatology clinical research experience
• Familiarity with GCP guidelines and FDA regulations governing clinical research
• Experience with CTMS, EDC, or eTMF platforms
• ACRP or SOCRA certification (CCRC or CCRP), or active pursuit of certification

About the company

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research. They have a network of 100+ sites across the US, Europe, India, and Australia.