Sort by
Refine Your Search
-
Country
-
Employer
-
Field
-
technical bases for potential new advocacy efforts, developing research strategies studies and scientific materials for rigor and soundness of scientific methodology (including statistical analysis
-
of chemical engineering principles including; reaction kinetics, chemical thermodynamics, heat and mass transport, engineering statistics, reactor design. Strong attention to detail in experimentation and
-
with tangential flow filtration Statistical software use, such as JMP Experience with GMP manufacturing Familiarity with CMC team function Experience with technology transfer to manufacturing Work
-
on deliverables throughout the process Provide input for the design of the Statistical Analysis Plan (SAP) and the clinical data output Responsible for review of patient level data across a study and for
-
with 3+ years experience or MA/MS with 0+ years related experience required. Experience working with MatLab, preferably working with image processing, signal processing, statistics or data/image
-
visualization / insights generation from data is easily accessible and understandable for users BASIC QUALFICATIONS Degree in Data Sciences , or Computer Sciences, Statistics, Clinical Informatics or similar
-
critical path experiments in alignment with team objectives Uses critical thinking to solve complex problems, address challenges and overcome obstacles Understanding of appropriate statistical design and
-
set-up. Proactively coordinate with Clinical Scientists and Lead Clinician to assure understanding and agreement on deliverables throughout the process Provide input for the design of the Statistical
-
-solving, risk analysis and statistical tools. Experienced in regulatory dossier compilation and developing CMC responses. Experience in supporting scale-up and technology transfer to pilot or commercial