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Senior Statistical Programmer Consultant, Oncology
ClinChoiceSenior Statistical Programmer Consultant leading programming activities for oncology clinical trials. Collaborating with internal teams and external vendors while ensuring quality deliverables in statistical programming.
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
SASSDTMADaMstatistical programmingdata derivationsdata analysesprogramming deliverablessubmission-ready outputsdefine.xmlannotated CRFs
Soft Skills
communication skillscollaborationleadershiptimeline managementquality assuranceattention to detailproblem-solvingcross-functional teamworkorganizational skillsstakeholder management
Tools & Technologies
CDISC guidelinesTables Listings Figures (TLFs)CROsexternal vendorsregulatory submissionsprogramming standardsdata management systemsbiostatistics toolsmedical writing toolsreviewer guides
Industry Keywords
oncology clinical trialspharmabiotechCROhematologic tumorssolid tumorsregulatory compliancedata qualityclinical study reportingstatistical analysis
About the role
Key responsibilities & impact- Lead programming activities for oncology clinical trials across multiple studies.
- Develop, validate, and maintain SDTM and ADaM datasets following CDISC guidelines.
- Oversee production of Tables, Listings, and Figures (TLFs) for study reporting and submissions.
- Provide SAS programming expertise to support complex data derivations and analyses.
- Review and ensure traceability, consistency, and quality of all programming deliverables.
- Act as programming lead for assigned studies, managing timelines and deliverables.
- Work closely with Biostatistics, Data Management, Medical Writing, and Regulatory Affairs.
- Coordinate with CROs and external vendors, ensuring compliance, quality, and adherence to client programming standards.
- Prepare submission-ready programming outputs and documentation, including define.xml, annotated CRFs, and reviewer guides.
Requirements
What you’ll need- Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field.
- 8–12+ years of statistical programming experience in pharma/biotech or CRO.
- Expert-level proficiency in SAS.
- Strong understanding of CDISC SDTM and ADaM standards.
- Significant experience supporting oncology clinical trials (hematologic or solid tumors).
- Experience supporting regulatory submissions and preparing submission-ready outputs.
- Excellent communication skills and ability to collaborate cross-functionally.
Benefits
Comp & perks- Health insurance
- Professional development opportunities
- Flexible work arrangements