Technical Writer

• Assist Scientists to prepare protocols, methods and reports for sponsors' studies;
• Organize study documents, such as, notebooks, sample receiving documents, CoAs of reference standards, etc., for individual studies;
• Compile and review all results from instruments and Watson-LIMS database for report writing;
• Able to use templates to prepare protocols and reports for scientists in an efficient manner.

• A minimum of a Bachelor's degree, with previous experience in a research laboratory
• Writing communication prefered
• Knowledge of GLP, cGMP, and ICH guidelines;
• Strong organizational and communication (written and oral) skills; and
• Knowledge of Microsoft^® Word, Excel, and Powerpoint.

Travel: None

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.