Description:
Writing various study reports using the provided protocol, execution documentation and statistical analyses in order to summarize the study purpose, procedure, evaluation, evaluation criteria, results, and conclusion for use in global regulatory submission documents.
Creating new or updating existing regulatory submission documents.
Qualifications:
Science degree
Previous experience working with regulatory submission documents
Previous experience in summarizing scientific studies
Excellent knowledge of Microsoft Word, including the use of templates, short cuts, and styles, and knowledge of creating and incorporating redlines into a clean copy
Excellent ability to learn new software applications
Experience in leading cross-functional teams to incorporate feedback into study reports and/or regulatory submission documents
#INDW3
Clear All
0 Medical Writer jobs found in Racine, WI area