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Medpace

Global CRO delivering full-service clinical trials

Medical Imaging Analyst

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeLeuven, BelgiumNo salary listed

About the Job

Requirements

  • A bachelor's degree in biomedical engineering, biomedical sciences, MBRT, or a similar field, with knowledge of medical imaging gained from performing, reviewing, or analyzing medical images in a research or clinical setting.
  • One to three years of experience in clinical research or an imaging-related field, including at least two years of experience in an imaging center.

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, including contouring structures, performing preliminary measurements of lesions and volumes, and converting imaging formats, across multiple modalities such as echocardiography, X-ray angiography, MRI, CT, ultrasound, and DXA, using proprietary and third-party software.
  • Assist in developing imaging protocols to obtain required study metrics based on clinical trial protocols.
  • Write technical documents in English related to study-required imaging procedures.
  • Compile and maintain project-specific status reports and timelines associated with imaging studies.
  • Perform project-specific tasks in compliance with Good Clinical Practices, regulatory requirements (21 CFR Part 11, GDPR, and HIPAA), applicable departmental and companywide standard operating procedures, and project-specific protocols.

Desired Qualifications

  • Experience working with clinical trials or within the pharmaceutical environment.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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