Dear Allstat, 

Please find below details of our latest contract Statistical Programming
vacancy. 

If this opportunity is of interest for you and would like to discuss it
further please send an updated CV to [log in to unmask] or contact me
on +44(0)207 7633 4824 

Our Client, a World Leading Pharma, are looking to employ a Senior SAS
Programmers with strong experience in Tables, Listings, Figures and Graphs
through phases I – IV. The contracts are initially 12 months with strong
opportunity for extensions. 

Job Purpose 

The Senior Statistical Programmer provides statistical software programming
solutions and their documentation to Biostatistics in general and to support
analysis and reporting of clinical trial and/or project data for regulatory
submission. They will support 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.

Primary Responsibilities and Accountabilities

•	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, pooled datasets, listings,
tables, and figures. 
•	Plan and perform programming, validation and documentation activities for
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.

Education/Qualifications
 
•	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

Experience, Skills, Knowledge

•	Strong SAS experience within a Clinical/Pharmaceutical environment 
•	Good knowledge of drug development process in particular on collection,
storing, processing and analysis of clinical trial data.
•	Has well developed planning and analytic abilities.
•	Communicates clearly and effectively in written and oral form.

If this opportunity is of interest for you and would like to discuss it
further please send an updated CV to [log in to unmask] or contact me
on +44(0)207 7633 4824 
  
Kind regards 

Ben Cowley 


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