Clinical Research Project 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 5,000 people across 40+ countries.

Responsibilities:

* Engage in clinical trial management on a day to day level;
* Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy;
* Compile and maintain project-specific status reports;
* Interact with the Sponsor, study sites, and internal associates;
* Create and maintain project timelines; and
* Coordinate project meetings and produce quality minutes.

Qualifications:

* Bachelor's degree in a health sciences field required;
* Prior experience as a Study Coordinator or within the pharmaceutical industry preferred; and
* Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.
* Fluency in English.

We kindly ask to submit applications in English & salary request in ARS.
			

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