QA GCP Associate

				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:

* Coordinate, conduct, track, and resolve external/Sponsor audits and internal system audits on company-wide basis;
* Support coordination, conduct, tracking, and resolution of Regulatory Authority inspections on company-wide basis;
* Coordinate, conduct, track, and resolve Quality Event Corrective Action/Preventative Action (CAPA) investigations on company-wide basis;
* May be responsible for other project and responsibilities as assigned.

Qualifications:

* Bachelor's degree in life sciences or nursing;
* Experience in a GCP regulated environment is preferred but GMP or GLP experience will be considered
* Excellent written and verbal communication skills
* Exceptional teamwork skills
* Ability to work independently.
			

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Medpace, Inc.

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