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:
* Provide day-to-day project support activities - maintenance of project-related files, corresponding with study teams, etc;
* Perform administrative duties in conformity with company policies and procedures;
* Coordinate and schedule meetings, provide meeting minutes;
* Maintain databases/project specific status reports;
* Support filing and quality control reviews of our internal regulatory filing system;
* Manage study supplies; and
* Perform other administrative tasks as needed.
Qualifications:
* Working towards a Bachelor's degree in a Life Science field;
* Excellent organizational, communication, and prioritization skills;
* Knowledge of Microsoft Office; and
* Availability to work a minimum of 20 hours per week in our Cincinnati, OH office.
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