Responsibilities: Subjects who discontinue within 7 days of dose reduction/interruption after experiencing a list of AEs. This listing might require data to be merged from AE, EX and DS domains. nalyse/tour data across multiple compounds and clinical studies from different phases to answer research questions. Requirements: 4+ years' experience as data analyst or SAS programmer in the pharmaceutical industry. Experience developing and validating specification file for SDTM and ADaM datasets. Experience programming and validating SDTM and ADaM datasets. Experience programming and validating TLGs from ADaM datasets. Experience programming and validating complex ad-hoc listings from SDTM and ADaM datasets. Multiple listings will require complex merges from 3 or more domains sometimes from SDTM and ADaM. Experience developing and validating complex macros. Experience in developing datasets for Client/ISS submission. Experience in reading external data from txt/csv files, cleaning data and merging with existing SDTM/ADaM data. Experience in R or Python to execute models such as network, tree, cluster, regression, outlier, factor analysis, etc. Katalyst Healthcares and Life Sciences
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