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

Responsibilities

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

Experience Required

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

Compensation DOE - $130,000 - $180,000 base salary + benefits