Medical Imaging Analyst

Medpace, Inc.

Denver (CO)

On-site

USD 60,000 - 120,000

Full time

14 days+

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Benefits offered by this job

Medical benefits
Dental benefits
Vision benefits
401(k) plan
Vacation policy
Work from home flexibility

Job summary

Medpace is seeking an Imaging QA professional to ensure protocol compliance in medical imaging data collected during clinical trials. You will perform image processing across MRI, CT, US, and other modalities, help develop imaging protocols, and document imaging procedures in English.

The role involves compiling reports, maintaining timelines, and ensuring adherence to GCP, 21CFR Part 11 and SOPs, with opportunities for professional growth within a global CRO.

Qualifications

  • Bachelor’s Degree in biomedical engineering, biomedical sciences (or similar field), 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

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 (converting imaging formats, contouring, performing preliminary measurements of lesions and volumes) across multiple modalities 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

Skills

Medical imaging knowledge
Clinical research experience
Imaging analysis

Education

Biomedical engineering degree
Experience in clinical imaging

Job description

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 (converting imaging formats, contouring, performing preliminary measurements of lesions and volumes) across multiple modalities (including but not limited to MRI, CT, US, ECHO, DXA, etc.) 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 in biomedical engineering, biomedical sciences (or similar field), 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
TRAVEL:

Minimal

Compensation

A target salary range of $60,000 - $120,000 with potential for bonus awards. Your compensation will be based on your skills and experience. Medpace offers the following benefits for full-time 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, pet insurance, and reimbursement for travel expenses (including food and gas allowance, rental cars, and hotel accommodations).

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting‑edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross‑functional collaboration.

Purpose‑Driven Work
  • Work alongside physicians, scientists, and industry‑leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
  • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
  • Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
  • Office based environment with on‑site mentors
  • Defined career paths with clear advancement opportunities
  • Industry renowned onboarding and training programs designed to accelerate professional development
  • Ongoing training and continuous learning opportunities throughout your career
  • An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
  • Competitive compensation programs that recognize and reward performance
  • Comprehensive health, wellness, retirement, and PTO benefits
  • Office based culture with occasional WFH that provides flexibility for eligible positions after training
  • Company‑sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

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