Statistical Programmer
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Location
Michigan
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Sector:
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Salary:
Negotiable
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Contact:
Jessica Charles
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Contact email:
Jessica.Charles@volt.eu.com
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Job ref:
78039-PHARM-JCH_1614091734
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Published:
about 3 years ago
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Expiry date:
2021-04-24
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Startdate:
ASAP
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Consultant:
ConsultantDrop
Responsibilities;
- Produce/Quality Control (QC) randomization lists (implement randomization plan)
- Create/QC SAS data sets and associated documentation for internal use and for regulatory submission (e.g., CDISC, SDTM and ADaM)
- Annotate/QC annotation of CRFs for submission data sets and publishing of annotated CRFs
- Produce/QC TFLs from mock shells
- Review CRFs and eCRFs for programming implementation
- Review EDC data export downloads for compliance with export specifications
- Perform EDC user acceptance testing (UAT) for programming implementation
- Maintain awareness of developments (e.g., version differences, enhancements, changes) within SAS software
Requirements;
- MSc/PhD in Statistics, or equivalent
- 5+ years experience in clinical trials
- Proficient in SAS with a good basis of knowledge of statistical procedures.
- SAS Base Programming Certificate