Celerion - Senior Clinical Statistical Programmer
Upload My Resume
Drop here or click to browse · Tap to choose · PDF, DOCX, DOC, RTF, TXT
Requirements
• Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing related field. • Minimum 3 years of hands-on statistical programming experience in a CRO or pharmaceutical clinical trials environment. • Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/ODS. • Experience applying CDISC requirements to generate ADaM datasets and supporting documentation (define.xml, Reviewer’s Guides), demonstrating proficiency in these areas. • Familiarity with Pinnacle 21 validation. • Experience in early-phase clinical trials. • Experience with Phase I Safety, PK/PD analysis programming. • Strong problem-solving and decision-making abilities. • Demonstrates a high level of attention to detail. • Demonstrated ability to work collaboratively as part of a team. • Familiarity with R, Python, and other programming languages is preferred.
Responsibilities
• Independently develop, maintain, and process SAS programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures, • Perform peer QC, double programming and validation functions for statistical outputs from studies. • Lead statistical programming activities on studies and deliverables. • Assist Management and Biostatisticians with complex projects. • Design and implement SAS programs for standardized use. • Train and mentor junior programmers. • Ensure compliance with study protocol and departmental procedures.
Similar Jobs
No credit card. Takes 10 seconds.