Anavex Life Sciences Corp. is seeking an experienced professional with a strong background in SAS programming and data analysis. The successful candidate will have the opportunity to work on exciting projects and contribute to successful new drug development. Key Responsibilities * Responsible for developing and maintaining programming and validation specifications for TLGs as per requirements provided by the Biostatistician. * Create and maintain SAS programs to produce outputs to support the analysis and reporting of clinical trials. * Develop analysis datasets for trial-level reporting and integrated safety and efficacy activities. * Program and QC data listings, summaries, and Graphs as defined in SAP. If required, validate the statistical models used for programming. * Develop re-usable utility macros to build a macro library to support programming tables, listing, and graphs for phase 1-4 clinical trial reporting. * Collaborate with the project team to ensure the deliverables are completed on time with high quality. * Create submission-ready standard data presentations and data sets using standard coding and following standard industry processes, including SDLC. * Maintain all project documentation as required by SOP and Processes. * Mentor Statistical Programmers. * Ensure compliance with eClinical Solutions and industry quality standards, guidelines, and procedures. * Other duties as assigned. Position will be filled at level commensurate with experience. Requirements * Bachelor of Science degree in Statistics or related science preferred. * Minimum 3+ years in the Pharmaceutical/Biotechnology industry or equivalent work experience. * Experience in preparations for NDA filings. * Knowledge of CDISC related data models like SDTM and ADaM. * Experience working on multiple clinical protocols at the same time. * Excellent verbal and written communication skills. * Detail-oriented, ability to multitask with strong prioritization, planning, and organization skills. * Experience in extracting, manipulating, merging, summarizing, analyzing, and presenting data using SAS procedures. * Strong experience in base SAS programming, Proc SQL, macro programming, ODS, and various SAS modules: SAS/GRAPH, SAS/STAT, and other modules like SAS/Connect and SAS/Access is a must. * Experience with reporting environments and reporting tools related to SAS programming in the pharmaceutical industry; proc report, proc summary and proc tabulate. * Experience in working with relational databases and performance tuning of SAS programming is a plus. Remote position.