Current jobs related to Clinical SAS Programmer - Fairfield - Penfield Search Partners

Contact: Linda Aronova – laronova@penfieldsearch.com

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Responsibilities:

• Independently develop/validate programs that generate SDTM and analysis datasets based on ADaM specifications.
• Prepare/QC ADaM datasets documentation: Define.xml, Reviewer’s Guide and analysis metadata report.
• Independently develop/validate programs that generate tables and listings specified in the protocol or the Statistical Analysis Plan (SAP)
• Perform quality control on final reports.
• Provide QC and validation reports.
• Support development of technical programming specifications for ADaM standards
• Communicate with programming and statistics leads, data managers and other team members.
• Provide project progress updates of programming activities.

Requirements:

• BS/MS in Statistics, Biostatistics, Computer Science, Mathematics or Life Sciences
• 10+ years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry
• Strong SAS programming skills required in Windows & UNIX environment with proficiency in SAS/Base, SAS Macros, SAS/Stat
• Knowledge of working in SAS Grid environment with experience in SAS Enterprise Guide and SAS Studio is a plus.
• Experience with all clinical phases I, II, III and IV of trials is desirable.
• Good understanding of standards specific to clinical trials such as CDISC, SDTM, ADaM, MedDRA, WHODRUG
• Strong problem-solving skills
• Good organizational and time management skills
• Excellent communication skills and capability of communicating technical concepts.
• Excellent organizational skills with demonstrated success to multi-task and deliver viable solutions in a fast-paced environment with changing priorities.