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SeniorFull-time
Salary Range
$86,190 - $116,610 /year
This salary is estimated based on similar roles. The actual salary may vary.
About the Role
ClinChoice is seeking a Statistical Programmer Consultant to join a client team. This role combines technical leadership with project management, focusing on oncology clinical trials and regulatory submissions.
Key Responsibilities
- →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
- →Provide SAS programming expertise for complex data derivations and analyses
- →Review and ensure 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 teams
- →Prepare submission-ready programming outputs and documentation
- →Ensure all programming meets regulatory requirements (FDA, EMA, PMDA)
Requirements
- ✓Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field
- ✓6–10+ 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
- ✓Experience supporting regulatory submissions and preparing submission-ready outputs
- ✓Excellent communication skills and ability to collaborate cross-functionally
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