<http://schema.org/description>
"...The Clinical Scientific Expert I is responsible for ensuring the collection, review/reporting of high quality trial data, and study reporting/publishing in compliance with Novartis processes, GCP/ICH and regulatory requirements. In addition, responsible for ensuring high quality scientific inputs (under supervision) to the clinical development process and support program level activities as assigned.\n\n\u2022 In collaboration with Trial Statistician, support development of Reporting and Analysis Pla..."^^<http://www.w3.org/2001/XMLSchema#string>
<https://tapwage.com/city/1257431-sangareddi-india/pharma-biotech/jobs>