Client- Abbvie
100% remote position
- More than 6 years of SAS programming experience supporting Phase 1-4 clinical trials in CRO or pharmaceutical industry. Enterprise Guide experience is a plus.
- Solid CDISC Standards knowledge, 6+ years of ADaM programming experience supporting safety and efficacy analysis. Neuroscience TA experience is preferable but not required.
- Well experienced in converting information from aCRF, SDTM data, SAP into ADaM specifications and review TLF outputs from vendors.
- Experience on creating Tables, Listing and Figures for clinical study report using proc report or data _null_.
- Knowledge of regulatory submission process, experience on creating ISS, ISE ADaM datasets and TLFs is a plus.
- Team player with excellent communication skills and experience working with statistical programmers, statisticians and data management personnel.
* Education; Bachelors degree required, Master's nice to have.
Job Type: Contract
Pay: $25.00 per hour
Work setting:
- Remote
Experience:
- HEDIS: 1 year (Preferred)
License/Certification:
- Epic Certification (Preferred)
Work Location: Remote