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 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 successful candidate will develop and validate an automated next generation IVD sequencing system based on Ion Torrent technology with the objective of meeting FDA regulatory requirements for commercialization.
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.
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.
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).
He/She will be responsible for development and transfer efforts. In particular, performing laboratory studies, and writing and implementing SOPs and technical reports for the feasibility, design freeze and verification of new molecular products.
The primary responsibility of the role is to create and maintain the informatics structure for capturing experimental data generated for RD experiments, automate analysis of such data sets across a diverse set of projects, provide QC assessments of the data and pre-defined analysis.