Entry/Experienced Clinical 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; 
* Update CTMS with study milestones, enrolment projections etc. 
* Update eTMF and perform ongoing eTMF QC;
* Support clinical trial manager to draft study plans and study specific guidance documents;
* Manager site feasibility, site activation preparation and study supply managements;
* Communicate with regional cross functional team, vendors and sponsor effectively;

Qualifications:

* Bachelor's degree in a health sciences field;
* Prior experience as a Study Coordinator or within the pharmaceutical industry;
* Maintain thorough knowledge of project and ability to coordinate/present at internal/external meetings and conference calls;
* Excellent computer (word-processing, databases, Excel, Windows) and organizational skills.
			

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