In this role, you will be responsible for working closely with peers, Clinical Affairs management, R&D, Data Management, and Marketing groups to design study-related documentation, protocols and study reports for various types of diabetes-related studies. Must possess technical writing, communication, and monitoring skills, including organizational skills.
The focus will be on cellular and animal models of fatty liver disease, inflammation and fibrosis, including signaling pathways, transcriptional regulation and disease pathway modification with Intercepts therapeutic approaches.
Support all scientific aspects of clinical trial(s) and program level activities as assigned, providing scientific expertise to study protocols, case report forms, statistical analysis plans, interpretation of results, clinical study reports, graphical displays.
In this role, you will be responsible for the oversight of a number of projects primarily within the ORU PDM group providing scientific leadership and strategic direction to assigned projects from idea to POC.
The successful candidate will have a background and expertise in inflammation, immunology, and/or immuno-oncology as it relates to lymphocyte biology, especially T cell biology (NK/Macrophages cell biology is preferred).
In this role, the selected candidate will lead design, creation, implementation, optimization, analysis and results interpretation of diagnostic assay products supporting the development of companion therapeutic products.
This position is key to scientific research and developing, updating and maintaining assessment tools, for all KF lines of business, from Search to Leadership and Talent Consulting, to Recruitment Process Outsourcing (Futurestep).
In this role, the selected candidate must have a direct experience in determining the success of cell transfection using techniques such as reporter gene assays, protein analysis (western blot), real-time qPCR for mRNA quantitation, enzymatic assays, etc.