Joette Keen is responsible for the implementation and delivery of KCR’s Data Management (DM) and Statistics Services. Mrs. Keen brings to KCR more than 30 years of extensive experience in clinical data management, DM systems, as well as international operations management. Prior to joining KCR, Mrs. Keen worked at a global CRO supporting all areas of global technical solutions within DM. Before this Mrs. Keen spent 32 years at Merck and Co., where she held various positions in clinical Data Management and IT. Over the course of her career, Mrs. Keen was involved in many efforts across various functional areas within the Merck Research Labs. Her technical responsibility included developing data capture programs for paper based early and late phase drug and vaccine clinical trials, and SAS programs to transform the entered data for transmission to clinical databases. In one of her management roles at Merck, Mrs. Keen assumed full responsibilities for process design, implementation as well as quality assurance and continuous improvement in clinical DM.  

  Biochemical and Microbial Toxicology