Location
San Antonio, Texas
The role involves planning, designing, and producing scientific content for clinical and regulatory documents. It also includes managing and reviewing medical writing for study protocols, statistical analyses, and study reports.
A Master's degree in a related field and two years of related experience are required. Candidates must demonstrate strong organizational skills and proficiency in Microsoft Office software.
Responsible for planning, designing, monitoring, coordinating, analyzing and producing scientific content for clinical and regulatory documents. Manages and reviews medical writing of study protocols, statistical analysis and study reports.
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