UT Health San Antonio
Location
San Antonio, Texas
The role involves planning, designing, and analyzing scientific content for clinical and regulatory documents. It also includes managing the medical writing of study protocols, statistical analyses, and study reports.
A Master's degree in a related field is required, or a Bachelor's degree with four years of experience. Preferred backgrounds include scientific research in microbiology, biotechnology, or physics.
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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