Associate Director/Director- Site Contracts

				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 5,900 people across 40+ countries.

Responsibilities:

This role will be responsible for the strategic development of the group, management of the team, and continuous improvement of processes. As a leader of the Site Contracts team you will be responsible for providing input on new business development opportunities, developing and maintaining relationships with clients, and providing guidance and support to those negotiating site contracts and budgets.  A general understanding of study start-up and how the role of site contracts is integrated with other clinical operations functions is preferred.

Qualifications:

* Bachelor's degree;
* At least 8 years of contract management experience in clinical research, preferably at a CRO;
* Experience managing a group;
* Excellent communication, negotiation, and leadership skills; and
* Fluent in Japanese and English
			

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