
Senior Statistical Programmer – Sponsor Dedicated
Fortrea
full-time
Posted on:
Location Type: Remote
Location: Poland
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Job Level
About the role
- Review SAPs and TFL shells from a programming perspective.
- Advise on the development of complex TFL shells from a programming perspective.
- Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets.
- Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform quality control of SDTM, ADaMs and TFLs.
- Produce / define XML / PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs.
- Respond to QA and client audits and support qualification audits.
- Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business.
Requirements
- Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc.
- Solid professional experience as a statistical programmer within a biotech, CRO or pharmaceutical company.
- Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs.
- Proven professional experience with SDTMs, ADaM datasets (safety and efficacy) and TFLs.
- Solid knowledge of CDISC standards.
- Business fluency in English – both spoken and written – is a must.
Benefits
- Flexible work arrangements
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
SASSAS macrosSAS/STATSDTMADaMTFLXMLPDFAnalysis Results Metadata (ARM)debugging
Soft skills
communicationproblem-solvinginnovationquality controlefficiency improvement