Statistical Programmer

Location: Michigan, USA
Job Type: Permanent
Specialisation: Life Sciences
Salary: Negotiable
Reference: 78039-PHARM-JCH_1614091734
Contact: Jessica Charles
Email: email Jessica
My client a small niche CRO in the US who are currently looking to expand their Biometrics department across the US. They are looking for up to 3-4 Statistical Programmers at all levels. The roles can be home-based anywhere across the US.


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