| We are in search of a well-rounded team player that is interested in interfacing with a team of multidisciplinary collaborators (e.g. chemistry, neuroscience, pharmacology, immunology). Being creative, flexible, self-motivated, and able to problem solve are key skills in our lab. 75%
Responsible for the performance of flow cytometry and sorting analysis including all aspects associated with performing these studies. Specific techniques include, but are not limited to, PBMC (peripheral blood mononuclear cell) isolation, fluorescent dye chemistry, and multiparameter flow cytometry or sorting (FACS). Assist with preparation of samples and conduction of analysis by sequencing. Coordinate clinical and pre-clinical specimen management. All associated project development, preparation, problem solving, data analysis, etc. Support the clinical work and preclinical work being performed in the lab. Ensure that components of projects are completed in an ethically, scientifically rigorous, and timely manner. Provide technical expertise to research lab staff regarding problem solving, experimental procedures, statistical analysis, and research project design.
15%
Responsible for the performance of flow cytometry and sorting analysis including all aspects associated with performing these studies. Specific techniques include, but are not limited to, PBMC (peripheral blood mononuclear cell) isolation, fluorescent dye chemistry, and multiparameter flow cytometry or sorting (FACS). Assist with preparation of samples and conduction of analysis by sequencing. Coordinate clinical and pre-clinical specimen management. All associated project development, preparation, problem solving, data analysis, etc. Support the clinical work and preclinical work being performed in the lab. Ensure that components of projects are completed in an ethically, scientifically rigorous, and timely manner. Provide technical expertise to research lab staff regarding problem solving, experimental procedures, statistical analysis, and research project design.
10%
Writing or reviewing confidential or non-confidential study reports (manuscripts, posters, etc.). Presentations of relevant data or scientific papers. Reviewing and/or drafting CDAs, SOWs, and other CPS-related legal and technical agreements. Help with IRB submission and maintenance. Follow project execution and ensure timely delivery of results. Aiding other lab members with in vivo or in vitro tasks as needed. Assisting with NIH grant submissions and applications for regulatory compliance. |
