Nuclear Medicine Technologist

Medpace; Denver (CO); On-site; USD 70,000 - 120,000; Full time

Job summary

A leading clinical research organization is seeking a full-time Nuclear Medicine Technologist in Denver. This role involves performing quality assurance checks on medical imaging data, developing imaging protocols, and ensuring compliance with clinical practices. The ideal candidate will have a Bachelor's degree and relevant experience in clinical research or imaging. Competitive compensation and benefits are offered.

Benefits

Flexible work environment

Competitive PTO packages, starting at 20+ days

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Structured career paths with opportunities for professional growth

Discounts on local sports games, fitness gyms and attractions

Modern, ecofriendly campus with an on-site fitness center

RTD Eco Pass

Qualifications

• 1-3 years of experience in clinical research or imaging related field.
• At least 2 years of experience in an imaging center.

Responsibilities

• Perform quality assurance checks on medical imaging data.
• Develop imaging protocols for clinical trials.
• Write technical documents related to imaging procedures.

Skills

medical imaging

clinical research

quality assurance

Education

Bachelor’s Degree

Job description

Job Summary

Our imaging services are growing rapidly, and we are currently seeking a full-time, office-based Nuclear Medicine Technologist to join our team. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

• Perform quality assurance checks on medical imaging data collected during medical and device clinical trials to ensure protocol specific requirements are met;
• Perform established image processing techniques (c onverting imaging formats, c ontouring, performing preliminary measurements of lesions and volumes) using proprietary software as well as other third party software;
• Assist in developing imaging protocols to obtain required study metrics based on clinical trial protocols;
• Write (in English) technical documents related to the study required imaging procedure
• Compile and maintain project-specific status reports and project timelines associated with imaging studies; and
• Perform project specific tasks in compliance with Good Clinical Practices (GCP), regulatory requirements (21CFR Part 11), applicable departmental and companywide SOPs, and project specific protocols

Qualifications

• Bachelor’s Degree and ARRT credentialed, with knowledge of medical imaging from experience performing, reviewing, and/or analyzing medical images in either a research or clinical setting.
• 1-3 years of experience in clinical research or imaging related field, with at least 2 years of experience in an imaging center
• Experience working with clinical trials or within the pharmaceutical environment is preferred

Compensation

A target salary range of $70,000-$120,000/year. Your compensation will be based on your skills and experience. Medpace offers the following benefits for eligible positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, and pet insurance. For more details, please discuss with your recruiter.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Denver Perks

• Denver Office Overview
• Flexible work environment
• Competitive PTO packages, starting at 20+ days
• Competitive compensation and benefits package
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Community involvement with local nonprofit organizations
• Structured career paths with opportunities for professional growth
• Discounts on local sports games, fitness gyms and attractions
• Modern, ecofriendly campus with an on-site fitness center
• RTD Eco Pass
• Secure bike storage room

Awards

• Named a Top Workplace in 2024 by The Cincinnati Enquirer

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

EO/AA Employer M/F/Disability/Vets

• Bachelor’s Degree and ARRT credentialed, with knowledge of medical imaging from experience performing, reviewing, and/or analyzing medical images in either a research or clinical setting.
• 1-3 years of experience in clinical research or imaging related field, with at least 2 years of experience in an imaging center
• Experience working with clinical trials or within the pharmaceutical environment is preferred

Compensation

A target salary range of $70,000-$120,000/year. Your compensation will be based on your skills and experience. Medpace offers the following benefits for eligible positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, and pet insurance. For more details, please discuss with your recruiter.

• Perform quality assurance checks on medical imaging data collected during medical and device clinical trials to ensure protocol specific requirements are met;
• Perform established image processing techniques (c onverting imaging formats, c ontouring, performing preliminary measurements of lesions and volumes) using proprietary software as well as other third party software;
• Assist in developing imaging protocols to obtain required study metrics based on clinical trial protocols;
• Write (in English) technical documents related to the study required imaging procedure
• Compile and maintain project-specific status reports and project timelines associated with imaging studies; and
• Perform project specific tasks in compliance with Good Clinical Practices (GCP), regulatory requirements (21CFR Part 11), applicable departmental and companywide SOPs, and project specific protocols