A well-established, secure and commercially active biopharma is expanding its US statistical programming team. This is a project-level programming leadership role within a fully in-house function.

Responsibilities

• Lead programming delivery across assigned oncology studies
• Develop and validate SDTM, ADaM datasets and TFLs to submission standard
• Support data delivery for CSR packages and regulatory submissions
• Ensure alignment with CDISC standards and FDA/EMA requirements
• Contribute to programming process development and standards

Experience Required

• Bachelor's or Master's degree in a relevant discipline
• Strong SAS programming experience within pharma or biopharma
• Oncology experience required
• Demonstrable experience working directly for a sponsor company
• Solid working knowledge of CDISC standards (SDTM, ADaM)
• East Coast based only

Compensation DOE - $170,000 - $220,000 base salary + benefits