Job Summary :
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
What to Expect Next
Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Cardiologist - Medical Director to join our Core Labs in Leuven office. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success.
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.
- Participatie in training and subsequently demonstrating 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 the specific protocol requirements and Medpace’s SOPs.
- Blinded independent central review of ECG and cardiac imaging according to study endpoints as specified in clinical trial protocol, charter and according to GCP and standard Medpace SOPs.
- Participate in IntraReader and InterReader variability assessments.
- Participate in the development, review and evaluation of SOPs and study specific procedures.
- Must have an M.D. and current medical licensure.
- Specialization in Cardiology required.
- Experience with ECG and most cardiac imaging modalities and expertise interpreting ECG, Holter-ECG and one or more cardiac imaging modality and therapeutic application.
- Experience with various ECG and cardiac image analysis and viewing software (including PACS).
- Experience working with computer software including Word, Excel, Access and Project preferred.
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace? :
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Awards
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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