Overview:
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.
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 (e.g. contouring of structures, performing preliminary measurements of lesions and volumes, converting imaging formats) across multiple modalities (including but not limited to Echocardiography, X-ray Angiography, MRI, CT, US, DXA, etc.) using proprietary software as well as other third-party software;
* Assist in developing imaging protocols to obtain required study metrics based on clinical trial protocols;
* Write (in English) technical documents related to the study required imaging procedure
* Compile and maintain project-specific status reports and project timelines associated with imaging studies; and
* Perform project specific tasks in compliance with Good Clinical Practices (GCP), regulatory requirements (21CFR Part 11, GDPR, HIPAA), applicable departmental and companywide SOPs, and project specific protocols.
Qualifications:
* Bachelor's Degree in biomedical engineering, biomedical sciences, MBRT or similar field, with knowledge of medical imaging from experience performing, reviewing, and/or analyzing medical images in either a research or clinical setting.
* 1-3 years of experience in clinical research or imaging related field, with at least 2 years of experience in an imaging center
* Experience working with clinical trials or within the pharmaceutical environment is preferred.
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