Jobs · empllo
Associate Director, Statistical Programming
Keystone AI · North America · Posted 24d ago
About the role
Design and code SAS programs for clinical projects and produce CDISC datasets for regulatory submissions.
📋 Description Design and code SAS programs for clinical projects (BASE/SAS, SAS/STAT). Produce CDISC SDTM and ADaM datasets with specs. Develop and deliver TFLs and analysis to meet study/regulatory needs. QC SAS code and outputs for SDTM/ADaM datasets and listings. Create and review eCTD documents for regulatory submissions. Support integrated safety/efficacy datasets and ad hoc analyses. 🎯 Requirements MS in Statistics or CS; 6+ years SAS in pharma/biotech. BS in Statistics/CS with 8+ years pharma/biotech also considered. Proficient in SAS programming. CDISC SDTM/ADaM and FDA submission knowledge. Working knowledge of R preferred. Experience leading programming for early/late phase trials and NDA/MAA. 🎁 Benefits Remote work opportunities in the United States. Travel to Cambridge, MA several times per year. Accommodations available for candidates in the selection process.
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FAQ
Is the Associate Director, Statistical Programming role at Keystone AI remote?+
This Associate Director, Statistical Programming position is listed as remote (North America).
What is the salary for the Associate Director, Statistical Programming role at Keystone AI?+
The listing states 196000-219000 USD.
What seniority level is this Associate Director, Statistical Programming role?+
This is a senior level position.
How do I apply for the Associate Director, Statistical Programming role at Keystone AI?+
Use the "Apply on empllo" button to open the original posting on empllo, where you can submit your application directly to Keystone AI.