Nuclear Medicine Technologist-256453
Medix™ · Saint Louis, MO
FULL-TIME
Posted Sep 8, 2026
Job Description
About the Role
We are looking for a skilled Certified Nuclear Medicine Technologist (CNMT) who thrives at the intersection of direct patient care and scientific innovation. In this role, you will perform diagnostic imaging and therapeutic procedures while actively collaborating with our Principal Investigator (PI) to design, coordinate, and execute pioneering clinical research studies.
Key Responsibilities
- Administer diagnostic and therapeutic radiopharmaceuticals under physician supervision, perform PET imaging, handle equipment calibrations/QC, and maintain rigorous radiation safety standards.
- Partner with the PI on study design, protocol development, manual prep, database setup, and Ensure all research strictly adheres to Good Clinical Practice (GCP), FDA, IRB, and institutional guidelines. Manage regulatory filings, protocol amendments, safety logs, and adverse event reporting.
- Build and maintain research databases, analyze study data in collaboration with the PI, and assist in drafting progress reports, presentations, and publications.
- Serve as the primary liaison between sponsors, PIs, and internal teams while training and mentoring research staff and imaging technologists on protocol execution.
Qualifications
- Active Certified Nuclear Medicine Technologist (CNMT) certification is required.
- 2 years of experience in nuclear medicine.
We are looking for a skilled Certified Nuclear Medicine Technologist (CNMT) who thrives at the intersection of direct patient care and scientific innovation. In this role, you will perform diagnostic imaging and therapeutic procedures while actively collaborating with our Principal Investigator (PI) to design, coordinate, and execute pioneering clinical research studies.
Key Responsibilities
- Administer diagnostic and therapeutic radiopharmaceuticals under physician supervision, perform PET imaging, handle equipment calibrations/QC, and maintain rigorous radiation safety standards.
- Partner with the PI on study design, protocol development, manual prep, database setup, and Ensure all research strictly adheres to Good Clinical Practice (GCP), FDA, IRB, and institutional guidelines. Manage regulatory filings, protocol amendments, safety logs, and adverse event reporting.
- Build and maintain research databases, analyze study data in collaboration with the PI, and assist in drafting progress reports, presentations, and publications.
- Serve as the primary liaison between sponsors, PIs, and internal teams while training and mentoring research staff and imaging technologists on protocol execution.
Qualifications
- Active Certified Nuclear Medicine Technologist (CNMT) certification is required.
- 2 years of experience in nuclear medicine.
Additional Details
- City
- Saint Louis
- State
- Missouri
- Country
- US
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