CRA Virtual Info Session Event - Clinical Operations - South Korea

				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:

Dependent on the position but may include;

* Communicating and collaborating on global study activities;
* Ensuring timely delivery of recurrent tasks, consistently, with a high degree of accuracy;
* Compiling and maintaining project-specific status reports within department-specific data management systems;
* Interacting with internal project teams, Sponsors, study sites, and third-party vendors;
* Coordinating project meetings and producing quality minutes.

Qualifications:

* Bachelor's degree, Masters or PhD in life science pr related field; 
* Previous experience in the Clinical Trial industry is welcome;
* Fluency in local language and excellent English.
			

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