Medpace, Inc.
Location
Cincinnati, Ohio
Assist scientists in preparing protocols, methods, and reports for clinical studies. Compile and review data from instruments and the Watson-LIMS database to ensure accurate documentation.
Requires a minimum of a Bachelor's degree and previous experience in a research laboratory. Candidates must possess knowledge of GLP, cGMP, and ICH guidelines along with strong organizational and communication skills.
Our bioanalytical services are growing rapidly, and we are currently seeking a full-time, office based Scientfic Technical Writer to join our team. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
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
Why Medpace?
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