SENIOR STATISTICAL PROGRAMMER (CONTRACT)
Senior Statistical Programmer – Welwyn Garden City
A unique opportunity has opened for a full time contract Senior Statistical Programmer with strong SAS programming skills with a clinical/pharmaceutical environment background. Your knowledge of drug development processes will provide statistical software programming solutions and their documentation to Bio statistics in general and to support analysis and reporting of clinical trial and/or project data for regulatory submission.
Supporting the Project Programmer in designing and implementing the statistical programming strategy on a project. The Senior Statistical Programmer coordinates and performs statistical programming activities such that agreed objectives, standards, deadlines and other requirements with respect to specifications, program development, quality assurance and report delivery are attained in accordance with applicable processes.
*Provide advice and support to the statistical team on programming activities related to analysis and reporting of assigned drug development study/project results. Assess and clarify requirements, provide statistical programming solutions and ensure their efficient implementation.
*Contribute to CRF development and data structures definitions for clinical trials. Ensure consistency and adherence to available standards.
*Ensure that user acceptance testing on the structure and quality of data provided by Data Management is performed. As appropriate, perform the user acceptance testing of data structure and execute data quality acceptance checks. Develop additional study-specific checks as required.
*Develop programming specifications and ensures consistency with the statistical specifications for analysis datasets (VADs), pooled datasets, listings, tables, and figures.
*Plan and perform programming, validation and documentation activities for VADs, pooled datasets, listings, tables, and figures according to specifications, with high quality and within agreed time lines.
*Ensure adherence to statistical programming standards, effective use of available standard programs and compliance with Standard Operating Procedures.
*Support regulatory submission specific activities, e.g. electronic submission creation.
*Maintain efficient interfaces with internal and external customers.
*University education (BSc or MSc) or equivalent in Statistics, Computer Science, Mathematics or other analytical field.
*Very strong knowledge of SAS programming language with SAS/Base, SAS Macro, SAS/Graph, SAS SQL and some SAS/STATS
*Good knowledge of English in a business environment
If this sounds of interest to you and you wish to submit an application or would like further information on this role or other opportunities, Please contact me on (+44) 121 616 3740 or email email@example.com.
Keywords: Statistical Programmer, Clinical Trials, Drug Development, SAS SAS/BASE, SAS Macro, SAS/Graph, SAS SQL SAS/STATS, Contract, Welwyn Garden City, UK
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Job Reference: STATROC_1565696749
Broadcast As: 143140
Salary To: Negotiable
Job Type: Full Time
Job Term: Contract
Job Industry: Jobs at Paramount
Recruitment Consultant: Paula Keville-Spain