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.

ACCOUNTABILITIES

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, SKILLS, KNOWLEDGE

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

BENEFICIAL

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