Infusion RN - Lubbock, TX - Per Diem

Iterative Health•Lubbock, TX

10d

About The Position

An Infusion RN at Iterative Health supports the daily execution of clinical trials at a research site. The role combines patient care with study coordination, helping ensure protocol compliance, accurate records, and a positive experience for study participants. The RN works with the study team, principal investigator, sponsors, CROs, and participants in a fast-paced, protocol-driven environment. Responsibilities include coordinating and conducting patient visits, maintaining study documentation and CTMS records, supporting recruitment, and performing clinical procedures as specified by study protocols. As assigned, the RN places IVs, administers IV medications and fluids, gives injections, monitors patients during infusions, and discharges patients according to protocol and site policies. The role also supports data quality, participant safety, regulatory compliance, and protection of research participants’ rights and welfare.

Requirements

Active Registered Nurse (RN) license.
Solid nursing background, with a concentration in GI 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 organization 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 in accordance with protocol requirements.
Regularly enter relevant study and subject-specific information into the CTMS.
Complete and maintain study documentation, including consent forms, source documentation, progress notes, case report forms, and investigational accountability forms.
Review case report forms against patient medical records for completeness and accuracy and maintain them in accordance with FDA guidelines.
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 participants throughout their studies.
Dispense study medication, collect vital signs, and perform ECGs according to protocol.
Perform blood draws 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 in accordance with protocols and site policies.
Adhere to 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 involving access to, use of, and disclosure of PHI; 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 study status and results to management.
Perform other job-related duties as requested.