Clinical Project Manager

				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:

* Responsible for overall delivery of clinical study;
* Main point of contact for sponsors and study teams;
* Development of study-related documents;
* Attending and presenting at investigator meetings;
* Participation in project start-up activities (i.e., protocol review and implementation, kit supply ordering, coordination of kits, lab manual and requisition production and shipping);
* Day-to-day monitoring of project status through status reports and timeline documents;
* Providing support to research sponsors and clinical sites; and
* Occasional handling of biological samples is a possibility.

Qualifications:

*  Minimum Bachelor's degree in science or a health-related field;
*  Knowledge of Microsoft Office;
*  1 - 3 years of clinical laboratory experience; and
*  MT (ASCP) certification is preferred.
			

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