► «A damning
report on how the University of Minnesota (UM) protects volunteers in its
clinical trials concludes that researchers inadequately reviewed research
studies across the university and need more training to better protect the most vulnerable subjects,» Jennifer Couzin - Frankel
wrote Monday at ScienceInsider.
Experience
writing, editing, reviewing and formatting
clinical regulatory documents (e.g.
clinical study protocols,
clinical study reports and investigator brochures).