Administrative Assistant related to Clinical Trials for Clinical Monitoring

				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 5,900 people across 40+ countries.

Responsibilities:

* Provide day to day departmental support activities as necessary. Examples include: prepare, send, and store clinical trial related documents;
* Maintain database/spreadsheets to facilitate tracking/documentation of departmental activities;
* Conduct quality control reviews of departmental documents;
* Provide support to Clinical Research Associates (CRAs);
* Develop understanding of appropriate company Standard Operating Procedures (SOPs) and policies.

Qualifications:

* Native level Japanese (JLPT N1)
* Good English reading and writing skills;
* Minimum high school diploma and experience in health sciences or a business setting, bachelor's degree preferred;
* High knowledge of MS Word, Excel, and PowerPoint;
* High knowledge and organizational skills to perform day-to-day departmental support activities;
* Excellent communication skills.
			

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Medpace, Inc.

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