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Medpace

Global CRO delivering full-service clinical trials

Medical Reader - Cardiology

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

About the Job

Requirements

  • Must have an M.D. and current medical licensure.
  • Specialization in Cardiology is required.
  • Experience with ECG and most cardiac imaging modalities, including expertise interpreting ECG, Holter-ECG, and one or more cardiac imaging modalities and their therapeutic application.
  • Experience with various ECG and cardiac image analysis and viewing software, including PACS.

Responsibilities

  • Participate in oversight of assignments, training, and management of central readers of cardiac imaging and ECG.
  • Collaborate with Core Lab management on technical aspects of cardiac study assessments.
  • Participate in sponsor site visits and audits related to cardiac assessments as requested.
  • Participate in training and demonstrate competency in the operation of independent central review of ECG and cardiac imaging for clinical trials.
  • Review protocols, image review charters, and associated clinical and technical study documents as required.
  • Complete source documents accurately and promptly according to specific protocol requirements and Medpace's standard operating procedures.
  • Conduct blinded independent central review of ECG and cardiac imaging according to study endpoints specified in the clinical trial protocol and charter, and according to good clinical practice and Medpace standard operating procedures.
  • Participate in intra-reader and inter-reader variability assessments.
  • Participate in the development, review, and evaluation of standard operating procedures and study-specific procedures.

Desired Qualifications

  • Experience working with computer software including Word, Excel, Access, and Project is preferred.

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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