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:
* Maintain study-related documents;
* Attending study team calls;
* Primary point of contact for study teams and investigational sites;
* Preparing study metrics;
* Ensure that all aspects of designated clinical protocol are in accordance with project timelines, budgets and performance quality;
* Coordinate laboratory shipments;
* Compose and maintain departmental operating procedures and work instructions; and
* Interact with Project Managers, Sponsors, and vendors on project-related issues.
Qualifications:
* Min. Bachelor's degree in life sciences (e.g. Biomedical Sciences)
* Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.
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