Responsibilities :
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.
Qualifications :
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.
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