Medpace, Inc.
Location
Cincinnati, Ohio
The Clinical Trial Associate supports Trial Master File (TMF) oversight by ensuring all documents meet established quality standards, which involves managing electronic filing systems, tracking, maintaining, and performing quality checks on documents. This role also requires communication with internal associates globally regarding document errors and preparing documents for shipment.
Candidates must possess an Associate's degree or equivalent, with a Bachelor's degree being preferred, alongside some experience in document administration. Essential qualifications include high attention to detail, excellent organizational skills, strong written and verbal communication abilities, and knowledge of MS Office.
The Clinical Trial Associate supports TMF oversight for a trial by ensuring documents meet established quality standards. This position involves both independent and computer-based work, as well as opportunity for communication and collaboration with trial teams. Manage electronic filing system for trial documentation; Track, maintain, and perform quality check of electronic documents; Communicate with internal associates globally regarding errors in trial documents; and Prepare documents for shipment.
Associates degree, or equivalent required; Bachelor's degree preferred; Some experience in document administration; High attention to detail; Excellent organizational skills Strong written and verbal communication skills; and Knowledge of MS Office.
Why Medpace?
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