M

Medpace

Global CRO delivering full-service clinical trials

Radiologist - Core Labs

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

About the Job

Requirements

  • Must have an M.D. and current medical licensure.
  • Have experience with most medical imaging modalities and expertise interpreting one or more imaging modalities and therapeutic applications.
  • Have experience with various medical image analysis and viewing software (PACS) and using them for quantitative image assessments.
  • Be board eligible in Radiology or have equivalent training demonstrating competency.

Responsibilities

  • Complete source documents accurately and promptly according to specific protocol requirements and Medpace standard operating procedures.
  • Perform blinded independent central review of radiology examinations according to clinical study protocol endpoints, the study protocol and charter, good clinical practice, and Medpace standard operating procedures.
  • Review protocols, Image Review Charters, and associated clinical and technical study documents as required.
  • Participate in training and demonstrate competency in independent central radiological review of imaging for clinical trials.
  • Participate in oversight of assignments, training, and management of central readers.
  • Participate in inter-reader and inter-reader variability assessments.
  • Participate in sponsor site visits and audits as requested.
  • Collaborate with management to resolve technical, radiological, and study concerns and problems.
  • Participate in the development, review, and evaluation of standard operating procedures and study-specific procedures.
  • Perform other duties as assigned.

Desired Qualifications

  • Experience working with computer software including Word, Excel, Access, and Project.
  • Knowledge of radiological disease response criteria such as RECIST 1.1.

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

Recently Posted Jobs

Explore more opportunities at Medpace

See more jobs