SAS Programmer

Posted on: December 19, 2024

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.

Location

Remote position.