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SAS/Statistical Programmer - FTSE 10 - REMOTE - 3 Months+

Clement May

Posted on Jun 26, 2021 by Clement May

Southampton, Hampshire, United Kingdom
Immediate Start
Annual Salary

On behalf of a Global Leader we are currently looking for a SAS Statistical Programmer to join the partner on an initial 3 months + Contract.


  • Aid product design and development by establishing best approaches through statistics and design of experiments.

  • Apply SAS programming and analytical skills using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS

  • Being able to work with databases (SQL)

  • Provide advice and facilitate statistical analysis to scientists across R&D.

  • Design, develop, evaluate, validate, and modify computer programs using SAS to analyse pre-clinical, clinical and survey data.

  • Aid to the development of Statistical Analysis plans


Experience Required

  • Understanding of statistical methods and application of Data Standards to clinical and non-clinical studies.

  • Creation/QC of SDTM/ADaM dataset specification, datasets and TLFs (Tables, Listings and Figures) via using efficient SAS programming methodologies.

  • Highly proficient in Statistical SAS programming. Ability to develop SAS programming skills and related processes/procedures.

  • Provide the training to the staff or subordinates as/if required.

Technical/Functional/Leadership Skills Required

  • Liaise with CROs/Vendors for any statistical programming issues.

  • Proactive; self-driven with strong interpersonal, organizational, and multi-tasking skills.

  • Good communication/interpersonal skills.

  • Cross functional working and leading projects to deliver on time in full

Education/Qualifications/Certifications Required

  • Bachelor's degree in Computer Science, Statistics, Mathematics, other subject with high statistical content pharmaceutical/biotech or CRO setting using SAS with clinical and/or non-clinical experience


  • Experience in additional statistical software packages eg. Minitab/JMP, R, Python

  • Data Sciences knowledge

  • Experience with FDA regulatory submissions

  • Implementation of CDISC, CDASH and SDTM standards

Reference: 1238404369

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