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:
* Generate, revise, and maintain clinical documents;
* Coordinate quality control of documents and maintain audit trail of reviews and changes;
* Provide input on data analysis planning and its impact on clinical document outcome ; and
* Performs other duties and responsibilities as assigned.
Qualifications:
* Master's degree in a health or science-related field;
* Possess strong communication skills (oral and written);
* Intermediate knowledge of medical terminology and clinical patient management;
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