Manager, DPS Technology (Digital Pathology Solutions)

1 in 5 men and 1 in 6 women worldwide develop cancer during their lifetime, and far too many will lose their battle. At Navigate we envision a disease free world – our talented and passionate team is at the forefront of enabling drug development by using transformative science to deliver high quality, world class clinical biomarker solutions so we can one day realize that vision. Join us on our journey to turning innovative treatment ideas into reality to improve and extend patient lives across the globe. Navigate Biopharma, a fully owned subsidiary of Novartis, provides assay development, clinical trial testing, and companion diagnostics services to companies in the precision medicine field. At present, Navigate supports 100+ clinical trials from 30+ pharma, biotech, and diagnostic companies, including 8 of the top 15 oncology companies globally.<br> <br>As a Manager at Navigate, you will lead a team of scientists and guide the design, creation, execution, and troubleshooting of new assay procedures and follow GCP/GLP/CLIA regulations to support clinical trial sample testing. While part of a highly collaborative team, you will be accountable for the successful execution of multiple projects within the team. Ideal candidates are inspiring leaders and must demonstrate critical thinking, initiative and clear cross-functional communication. <br><br>Your responsibilities:<br>• Manage a team of 5-7 associates to plan & execute laboratory research, assay validation, and testing of patient specimens using multiplex fluorescence or chromogenic immunohistochemistry staining and digital image analysis methods<br>• Evaluate new technologies, testing platforms, software applications, novel biomarkers and leading implementation strategy.<br>• Analysis and QC of image data using software such as AQUA® Technology or HALO®, data transfer and reporting via LIMS.<br>• Interface with various cross functional teams and serves as subject matter expert.<br>• Interacts with internal or external sponsors representing specific projects including giving presentations.<br>• Follow all GMP/GCP/GLP/CLIA regulations and ensure Quality Events are documented<br>• Author and review technical documents such as work instructions, study protocols/reports and internal presentations. <br>• Using critical thinking skills, analyze data for trends making recommendations to scientific leadership team.<br><br>[#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}#/video#]