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Medpace

Global CRO delivering full-service clinical trials

Radiology Specialist Physician

Physicians & SurgeonsConfirmed live in the last 24 hours
Full-timeLeuven, BelgiumNo salary listed

About the Job

Requirements

  • A medical degree (M.D.) and valid recognition as a physician are required.
  • Radiology training and experience with medical imaging are required.
  • Knowledge of multiple imaging modalities and expertise in at least one area, such as CT, MRI, or PET, is required.
  • Experience with PACS systems and medical image-analysis software is required.
  • Interest in clinical research and applying radiology in drug development is required.
  • A precise, structured work approach with attention to quality requirements, study protocols, and standard operating procedures is required.

Responsibilities

  • Review radiological examinations in clinical studies according to the study protocol, specified evaluation criteria, Good Clinical Practice guidelines, and standard operating procedures.
  • Perform blinded, independent central image reviews, interpreting medical images consistently and objectively.
  • Evaluate imaging data according to study-specific endpoints and the study protocol's evaluation guidelines.
  • Complete study documentation and source documents accurately and on time, following protocol and standard operating procedure requirements.
  • Study and interpret study protocols, Image Review Charters, and related clinical and technical study documents.
  • Use medical image review systems, including PACS and specialized quantitative image-analysis software.
  • Participate in training for central radiological image review and demonstrate competence according to quality requirements.
  • Contribute to training, follow-up, and quality control of central reviewers, including inter-reader variability assessment, to maintain the reliability and consistency of reviews.
  • Collaborate with internal teams, project staff, and sponsors to resolve technical, radiological, and study-related questions and issues.
  • Help develop, review, and optimize standard operating procedures and study-specific procedures.
  • Participate in sponsor visits, quality checks, and audits as needed.
  • Perform additional duties within radiological review and clinical research.

Desired Qualifications

  • Experience with clinical studies, Good Clinical Practice guidelines, or RECIST 1.1 is a plus.
  • Familiarity with Microsoft Office applications such as Word and Excel is an advantage.

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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