Description

Lead statistical programming for early-phase clinical studies, focusing on oncology and PK/PD.

Responsibilities

• Develop SAS programs for analysis datasets, listings, and safety summary tables.
• Manage programming team deliverables at the study level, ensuring quality and timeline adherence.
• Create and maintain high-quality analysis dataset specifications and PDVD setups.
• Mentor junior programmers and act as a subject matter expert for complex SAS requirements.
• Liaise with Data Management and Medical Writing to facilitate project flow and support client-facing activities.

Required Skills

• 5+ years of experience in SAS programming.
• Oncology therapeutic area expertise.
• Experience in Phase I or early phase clinical trials.
• Pharmacokinetic and Pharmacodynamic (PK/PD) modeling experience.
• Working knowledge of CDISC SDTM and ADaM data structures.
• Experience with development and use of standard programs and macros.
• Proven track record leading programming teams in a client-facing capacity.
• Bachelor's degree in a quantitative or scientific discipline.

Key Skills

Education

Any Graduate