Dear Allstat
SRG Clinical is pleased to offer to the market a role within
Biostatistics & Programming Department with a clinical trials
organisation in Switzerland. Due to their continued success and an
extremely healthy pipeline they are seeking a Senior Programmer on a
permanent basis. If you wish to find out more about the nature of this
exciting role please send your CV to [log in to unmask] or call
Helena on +44 207 562 1792 or +44 7825 362548.
Senior SAS Programmer
Reporting into Director, Biostatistics your responsibilities will
include:
*
Providing programming input to CRF, SAP, analysis file
specifications, and tables, figures, and listings (TFLs) shells.
*
Writing SAS programs to generate derived analysis datasets,
perform analysis, and TFLs.
*
Performing ad hoc flexible and rapid programming arising from
questions generated from planned analyses and results.
*
Performing programming validation to ensure quality of analysis
datasets and programming outputs.
* Creating Data Definition Tables (DDT) and convert TFLs to the
required format for eSubmission.
*
Providing programming support for the preparation of
integrated reports, submissions and post-submission activities.
* Serve as a coordinator when multiple programming resources (e.g.
CROs or contractors) are used.
Skills/Knowledge Required:
* Bachelor's degree in life science, statistics, mathematics,
computer science, or related field required; Master's degree is
preferred.
* Significant Pharmaceutical/CRO experience as a SAS programmer
supporting clinical trials for regulatory submissions.
* Demonstrated proficiency in using SAS to produce derived
analysis datasets and TFLs.
* Have in-depth understanding of clinical data structure and
relational database.
* Demonstrated skills in using software tools and applications,
e.g., MS office, XML.
* Demonstrated ability in the handling and processing of upstream
data, e.g., multiple data forms, workflow, eDC, SDTM.
* Demonstrated ability in providing outputs to meet downstream
requirements, e.g., ADaM, Data Definition Table, e-submission.
* Have in-depth understanding of regulatory, industry, and
technology standards and requirements.
You must be eligible to work in the EEA and posses excellent written and
oral English skills. I look forward to your application.
best wishes
Helena
Helena Newman-Mitchell
Biometrics Lead
Direct: +44 (0) 207 562 1792
Fax: +44 (0) 207 562 1799
Mobile: +44 (0) 782 536 2548
Email: [log in to unmask]
Website: www.srgclinical.com <http://www.srgclinical.com/>
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