location_onRadnor, PA 19087, USA
watch_later Posted: Nov 21, 2024
Job Description
Requirements and scope:
- MS or PhD with 10-15 years in hands-on experience in biostats for biotech pharma.
- Strong SAS programming skills to perform stats validation on the key outputs directly from raw data to TLGs
- Strong knowledge and experience for multiple imputation for missing data and intercurrent events
- Ability to lead the SAS code development for the modeling
- Review SDTM, ADaM specs and ensure sound implementation of algorithms of vendor pipeline and internal validation pipeline
- Detailed technical skills related to mixed modeling, missing data imputation methods, sensitivity analysis, estimands
- Experience with ISS/ISE and NDA submissions with fast turnaround times.
- Drive the overall delivery timeline and organize cross functional reviews
- Works independently with minimal guidance
- Clear communicator and willing to keep up with rapid work pace
- Full time - 40 hours per week.
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