Lead programming activities within the Biometrics group to drive quality and compliance.
Oversee clinical programming deliverables and support regulatory submissions.
Mentor a team of statistical programmers and foster high performance.
Develop and validate SDTM/ADaM datasets per CDISC standards, with oncology focus.
Collaborate across Biostatistics, Clinical Data Management, Medical Writing, and Regulatory teams.

🎯 Requirements

Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, Life Sciences, or related field.
9–11+ years of statistical programming in pharma/CRO.
Strong SAS programming; knowledge of R is a plus.
Deep CDISC SDTM/ADaM expertise.
Experience with oncology clinical trials.
Proven leadership and mentoring of programmers.
Excellent communication and cross-functional collaboration.

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