Clinical Supply Chain Project Specialist (PharmD Candidates)

				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:

* As a member of CP&S department, support and collaborate in all activities related to investigational productsupply chain;
* Support CP&S department to translate clinical study protocol into investigational supply chain;
* Monitor alignment of CP&S timelines with project timelines;
* Attend teleconfrences with internal Medpace teams, Sponsors, and/or Vendors and communicate/present both virtually and face to face; and
* Support collaboration with Clinical Trial Manager other functional areas to provide study deliverables.

Qualifications:

* PharmD;
* Ability to escalate;
* Prioritization of daily, weekly, monthly, and project workloads;
* Stong communication and problem-solving skills;
* Effectively collaborate with internal and external colleagues;
* Provide excellent internal and external customer support.;
* Understand multiple potential solutions;
* Solid working knowledge of Power Point, Excel, Word; and
* Interest in a new experience in Medpace.
* Understanding of GCP, GMP, GxP is preferred
			

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