The successful candidate will collaborate with study teams working effectively to design studies, develop protocols, write statistical analysis plans, perform statistical analysis, write reports, present results summarizing findings, and develop publications of results.
In this role, you will apply novel computational analysis and biological interpretation approaches to leverage internal, public and partner datasets and empower data-driven decisions across therapeutic programs.
In this role, you will be responsible for leading process development activities to execute large molecule downstream processing including lab-scale process development, in-process assay support, and process scale-up/scale-down.
In this role, the selected candidate will manage multiple projects within Bioanalytical Operations (BAO). Work closely with groups within BAO, clinical teams and other working groups to establish project objectives and ensure they are achieved to support clinical development.
In this role, the selected candidate will build customer profiling and predictive models utilizing both traditional statistical methods (Generalized Linear Models, Mixed Effects Models, Ridge, Lasso, etc.) and modern machine learning techniques (Gradient Boosted Trees, Random Forests, Kernel methods, Deep Learning, etc.)
In this role, you will provide intricate analytic solutions to meet end user needs. Has various tool knowledge with both software development and engineering research to create models of relevancy. Experience designing efficient algorithms with programming languages and tools for data manipulation and statistical analysis. Experience designing efficient data mining and text mining frameworks with related tools.
In this role, you will drive a range of Applied Research and New Product Development projects by providing project leadership and direction. The selected candidate will prioritize group efforts to deliver on most important and most commercially significant projects.
In this role, you will be accountable for the maintenance of the electronic Trial Master Files (TMF) in accordance with NNI SOPs and performs ongoing reviews of TMF to assure quality of the documentation files and compliance with NNI SOPs, GCP and ICH Guidelines.
In this role, the selected candidate will be responsible for supporting the development of innovative drug delivery approaches, and feedback/observations from the analytical work will be sought to guide future work.
In this role, you will be responsible to lead and document product development lab work, including development of benchtop prototypes, implementation and maintenance of stability testing, and scale-ups for commercialization.