Senior & Principal Statistical SAS Programmers - Clinical Trials

Docs International UK Limited ,
London, Greater London
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Overview

As part of an ongoing global biometrics & data operations FSP with a TOP 5 pharmaceutical company, at DOCS Global (an ICON Clinical Company), we are continuing to recruit for experienced Clinical Trials Statistical SAS Programmers at Senior, Lead and Principal Levels. Roles can be offered as home based or office based across a number of EMEA countries. A minimum of 6 months of Statistical/SAS Programming experienced gained in EMEA region is essential to be considered for these roles. Title: Senior, Lead & Principal Statistical/SAS Programmers - Multiple Roles Duration: Full Time Employment Locations: Home Based (or office based) in several EMEA countries. Description: Bachelors degree or higher in Statistics, Computer Science, Life Sciences or other related areas. 6-10 years of experience in Programming using SAS, gained within Clinical Trials. Good hands on experience in developing data sets as well as TLFs (Tables, Listings and Figures). Also, in QC / Validation Programming. Experience in developing Macros. Experience in development of datasets and dataset specifications in line with internal standards and CDISC (ADaM and SDTM) Standards. Proven ability in coordinating and leading programming support activities for clinical trials and submissions. Experience in acting as a Study Programming point of contact and as a Lead Programmer / Trial Programmer on assigned studies. Working experience in pooling analysis datasets across multiple clinical studies Please note that we can not offer sponsorships for these roles, hence we can consider only those applicants with existing work rights for a EMEA country where we can offer these roles. For additional information about these roles including detailed job descriptions and/or to apply please get in contact with Pradeep Garepalli at Docs Global. This job was originally posted as www.totaljobs.com/job/89886877

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