Contract Senior SAS Programmer

  • Salary: £50-55 phr Umb Co.
  • REF Number: 00049539
  • Consultant:
  • Contact: 01246 457709
  • Date Published: 06.01.2021
  • Sector: Non-Specific
  • Location: Abingdon, Oxon/Wilts
  • Discipline: Biometrics

CK Group are recruiting for a Senior SAS Programmer to work for a Clinical Biometrics consultancy on a contract basis for 6 months initially. The role is home based and deemed outside IR35 but the client will only engage with freelancers via an Umbrella Co. Alternatively you can work through CK Group on a PAYE basis.

The Company: A Clinical Biometrics consultancy based in EU and UK. The client has a team of over 60 carefully selected and highly experienced staff has extensive expertise insupporting projects ranging from pre-clinical and clinical development, pharmaceutical licensing in the EU and US, medical technology research and other healthcare management activities.

Specialise in: Biometrics SAS and Statistical ProgrammingBiostats CDISC Regulatory Data Analytics/Management Project Management

The Role:

The main purpose of the role will be to

  • Review documents that have an impact on SAS programming
  • Perform SAS programming for efficacy and safety tables,listings, figures and analyses
  • Perform SAS programming for CDISC SDTM and/or ADaM datasets
  • Produce tables, listings and figures of data for reports (e.g. Clinical Study Reports, Statistical Reports, etc)
  • May produce CDISC associated files,such as Define.XML, reviewer’s guides and SDTM annotated CRFs
  • Perform QC of analysis datasets, tables, listings, figures and analyses
  • Perform SAS program software development and creates associated documentation
  • Write/update user documentation
  • May mentor other SAS Programmers
  • Maintain good working relationships with company colleagues at all times
  • Contribute to improving S-cubed Biometrics processes and promoting effective change

Your Background:

To succeed in this role, you will have the following experience (amongst others):

  • Excellent working knowledge of SAS, CDISC (both SDTM and ADaM) standards and other relevant software technologies.
  • Excellent level of proficiency in the full range of essential SAS programming tasks.
  • Fully conversant with the software development life cycle.
  • Knowledge of the pharmaceutical industry processes and regulations, with good understanding of clinical trials and the application of ICH GCP to SAS and SAS programming functions.

Entitlement to work in the UK is essential. For more information or to apply for this position, please contact Russell Oakley on 01246 457709 or email roakley@ckgroup.co.uk. Please quote reference 49539 in all correspondence.

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