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SAS programmer Statistical Programmer

South East, United Kingdom, £ £ 35000.00-78000.00 Annual Annual, Contract

Description:

SAS programmer Statistical Programmer c£35k-78k (prorata)

South Ref: ABJ5276

3 months contract

Approx £(Apply online only) a day ltd dependent on experience

INSIDE IR35

An experienced SAS programmer or Statistical programmer you will enable the delivery of the a risk program and provide statistical support and programming across R&D projects and to facilitate statistical programming to ensure robust and efficient scientific data analysis and reporting.

The group has been leading in the development of the scientific efficacy assessment of compounds and this SAS programmer supports regulatory engagement, compliance and new product categories. As a sas/statistical programmer you would be using data from pre-clinical and clinical studies to substantiate claims and to pass to regulatory submissions teams to help product launches and establishing partnerships and collaborations to develop new capabilities to enhance science delivery.

Key Responsibilities

* 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

Qualifications and Experience

* 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

* 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.

* Familiar with Statistical Programming, Computational Statistical Modelling, Data Mining

* Knowledge of data standards, implementation of data standards and regulatory compliance.

* experience in Pre-Clinical, Clinical, Non-Clinical Human Studies and Analytics

* Any exp in Pharmaceutical, Human / Psychological studies, Biomedical, Biotech or CRO?

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

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

* 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

To Apply: Please contact Alison Basson at Hudson Shribman Scientific Recruitment, Please call on (phone number removed) or (phone number removed) OR the job title and reference code ABJ5276 in the subject field to

Job Details

1328726077
Not Specified
South East, United Kingdom
Contract
£ £ 35000.00-78000.00 Annual Annual