Lead/Principal Statistical Programmer-(Oncology) Remote
Skills
- Proficient in SAS programming for clinical data
- Strong knowledge of FDA and CDISC standards
- Experience with SDTM, ADaM datasets and define.xml
- Good understanding of clinical drug development and regulatory guidelines
- Excellent leadership, communication, and coordination skills
Responsibilities
- Program edit checks for Data Management using SAS
- Create tables, listings, and figures for clinical study reports
- Annotate blank CRFs following FDA and CDISC guidelines
- Create or QC SDTM and ADaM datasets and specifications
- Prepare define.xml/pdf, cSDRG.pdf, and ADRG.pdf documentation
- Lead and manage programming teams and coordinate project delivery
- Integrate data across studies for ISS, ISE, and electronic submissions
- Mentor programming leads and managers following industry standards
Education
- Bachelor’s degree in Computer Science, Statistics, or related scientific disciplines with 10+ years clinical programming experience
- Or Master’s degree in relevant fields with 9+ years clinical programming experience
Benefits
- Opportunity to work remotely
- Professional development and continuous training
- Inclusive and diverse workplace culture
- Stable employment with a mature global CRO
- Work-life balance focused environment
Average salary estimate
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