Associate Director, Programming
Job Location: N/A
Essential Duties & Responsibilities:
Develop programming plan for statistical outputs (datasets, tables, listings, figures, etc.) supporting clinical study reports, regulatory submissions and publications including resource needs and timelines. Independently create SAS programs for statistical outputs. Independently perform quality control on statistical outputs created internally or by vendors. Design and oversee the programming of SAS macros to support statistical outputs within a project, within a development program, across projects and across development programs. Provide input into development of the SAS programming environment. Oversee the maintenance of the SAS programming environment. Manage the programming effort on a project. Provide support in managing statistical programming performed by vendors. Provide reports to Biostatistics management on the status of statistical programs and outputs. Manage programming resources and effort to timeline, alerting Biostatistics management to potential issues and delays. Provide CDISC expertise and ensure adherence to SDTM and ADaM standards. Provide SAS ODS expertise.
Required Education and Experience:
Master’s degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related field, and 8+ years of programming experience preferably in processing clinical trial data in the pharmaceutical industry, or Bachelor’s degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related field, and 10+ years of programming experience preferably in processing clinical trial data in the pharmaceutical industry.
Please contact Bill Emker at email@example.com
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