Infusion RN - Lubbock, TX - Per Diem

Iterative Health•Lubbock, TX

11d•$31 - $45

About The Position

An Infusion RN at Iterative Health supports clinical research trials at a research site, coordinating patient interactions and carrying out protocol-driven clinical procedures. The role includes administering IV medications and fluids, monitoring patients during infusions, and discharging them in accordance with study protocols and site policies. The RN also supports study operations, patient recruitment, documentation, data quality, and communication with research participants and study stakeholders. The position is part of Iterative Health’s site research team. The company operates a network of 100+ research sites across the US, Europe, India, and Australia and has more than 250 employees worldwide. Iterative Health is headquartered in Cambridge, Massachusetts, and New York City.

Requirements

Active Registered Nurse (RN) license.
Solid nursing background, with a concentration in GI specialty or willingness to develop advanced GI knowledge.
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.
Strong organizational skills and ability to manage multiple priorities and meet deadlines.
Ability to work independently and collaboratively in a fast-paced environment.

Nice To Haves

1–2 years of clinical research experience is strongly preferred.
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.

Responsibilities

Administratively and clinically manage industry-sponsored clinical trials, including problem-solving, communication, and protocol management.
Schedule patient research visits and procedures according to protocol requirements.
Enter study and subject-specific information into the CTMS regularly.
Complete and maintain study documentation, including consent forms, source documentation, progress notes, case report forms, and investigational accountability forms.
Maintain case report forms in accordance with FDA guidelines and review them against patient medical records for completeness and accuracy.
Schedule and prepare for monitor visits.
Maintain onsite inventory of study equipment and supplies.
Lead patient recruitment activities, including chart reviews, protocol discussions, and verification of informed consent documentation.
Conduct patient visits as outlined in study protocols and serve as the primary point of contact for study participants.
Dispense study medication, collect vital signs, and perform ECGs according to protocol.
Draw blood and process and ship specimens according to study protocols and IATA regulations.
As assigned, place IVs; administer IV medications and fluids; give intramuscular and subcutaneous injections; monitor patients during infusions; and discharge patients according to protocols and site policies.
Follow Research SOPs, Good Clinical Practice guidelines, and study protocols.
Assist with data verification and quality control to ensure data integrity and consistency with study protocols.
Ensure safety data is reviewed by the PI in a timely manner.
Cooperate with site compliance and monitoring efforts related to access, use, and disclosure of PHI, and report noncompliance to the appropriate compliance office.
Help protect the rights and welfare of human research participants in accordance with federal regulations.
Maintain communication with CROs, sponsors, research participants, the Site Manager, and the PI throughout each study.
Communicate status and results to management.
Perform other job-related duties as requested.