Experienced Clinical Trials Feasibility 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:

* Coordinate feasibility assessments and deliver high quality, accurate feasibility data to internal and external teams;
* Develop preliminary proposal strategy for site and country selection;
* Present feasibility results to members of the proposal team to assure correct assumptions were applied and strategy is in line with our therapeutic and operational experience;
* As needed to support feasibility strategy, coordinate outreach to investigative sites to obtain indication and protocol specific feedback;
* Assist with review of work developed by more junior feasibility coordinators;
* Collaborate with operational team members in preparation for bid defense meetings; and
* Support departmental process improvement initiatives and general departmental administrative functions.

Qualifications:

* Bachelors degree in life sciences required, Masters or PhD preferred;
* 3-5 years of feasibility experience within a CRO;
* Analytical thinker with great attention to detail;
* Ability to prioritize multiple projects and tasks within tight timelines; and
* Excellent written and verbal communication skills.
			

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