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:
* Create and maintain laboratory manuals (general and study-specific) and other study- related documents;
* Develop and present clinical laboratory presentations at investigator meetings;
* Design specifications and monitor production of specimen collection kits;
* Track study status as appropriate;
* Communicate all aspects of protocol to various internal departments for appropriate study setup, maintenance, and closeout; and
* Write, establish, and revise relevant Standard Operating Procedures and/or work instructions.
Qualifications:
* Bachelor's degree in science or a health-related field;
* Laboratory experience preferred;
* Excellent oral and written communication skills.
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