Clinical Safety Coordinator

				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 6,000 people across 40+ countries.

Responsibilities:

* Determine plan of action for incoming calls;
* Collect, process, and track incoming events;
* Write safety narratives;
* Report on various safety data; and
* Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.

Qualifications:

* Bachelor's of Science in Nursing;
* At least one year of clinical experience;
* Clinical Research/Post marketing Pharmacovigilance experience is preferred;
* Proficient knowledge of Microsoft(r) Office;
* Broad knowledge of medical terminology;
* Strong organizational and communication skills.
* Bilingual Japanese and English
			

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