This is a pre-market vacancy. The search will begin by the end of November '25. Apply now to be considered ahead of the rest of the market.

Role Summary

A clinical-stage oncology biotech is looking to engage an experienced Associate Director / Director of Statistical Programming to lead programming strategy and execution across key clinical trials.



Responsibilities:

• Serve as the programming lead across multiple studies, including pivotal trials in oncology.
• Develop and validate SDTM, ADaM, and TLFs in support of both ongoing studies and regulatory submissions.
• Oversee CRO programming deliverables, ensuring high quality, accuracy, and compliance with timelines.
• Partner closely with Biostatistics, Clinical Development, Data Management, and Regulatory to ensure alignment on programming needs and strategy.
• Support data delivery for CSR packages, regulatory submissions, and exploratory analyses.
• Contribute to process development, documentation, and implementation of programming best practices.
• Act as a key technical advisor on submission readiness and data standardization.

Requirements:

• Bachelor’s or Master’s degree in a relevant field
• Extensive SAS programming experience within the biotech/pharma sector, ideally with oncology exposure.
• Strong working knowledge of CDISC standards (SDTM, ADaM) and submission requirements.
• Track record of managing CROs and delivering study-level programming outputs.
• Excellent communication skills and ability to operate effectively in a cross-functional, fast-paced setting.

Salary based on experience and will be provided after search kickoff