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:
* Develop, program, validate and maintain clinical trial databases according to company standards;
* Maintain and contribute to company library of standard CDASH compliant CRFs ; and
* Act as primary contact to the data management team for assigned studies, supplying all necessary technical support, and ensuring quality of the programming and adherence to company standards.
Qualifications:
* Bachelor's degree/Advanced degree in Life Sciences or Computer Science or equivalent;
* 2-3 years of Rave study build experience in a similar position in Pharma/Healthcare sector;
* Custom function (C# Programming) experience is preferred;
* Certified Medidata Rave Study Builders preferred;
* Excellent verbal and written communication skills; and
* Meticulous attention to detail.
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