Senior Programming Lead, Oncology

What you'll do

• Plan, coordinate, and oversee the execution of programming activities for one or more clinical trials.
• Design and develop programs to support complex clinical data analysis and reporting activities.
• Create and deliver CDISC-compliant data packages and reviewer’s guides for submission activities.
• Provide technical guidance and leadership to programming teams to ensure high-quality, on-time deliverables.
• Manage outsourced programming activities by third-party vendors to ensure they meet scope, timeline, and quality standards.
• Implement metadata-driven approaches and create efficiencies in clinical data flow across trials.
• Lead departmental innovation projects to develop and implement new processes, systems, and tool improvements.

What we're looking for

• Bachelor’s degree or higher in computer science, mathematics, data science, public health, or a relevant scientific field.
• 4+ years of experience in programming and/or clinical data management, preferably in a pharmaceutical or clinical trial environment.
• Knowledge of programming practices, data structures, and languages for data manipulation, statistical analysis, and reporting.
• Proficiency in SAS is required.
• Knowledge of CDISC standards is required.
• Experience in planning and coordinating programming activities and leading teams is required.
• Working knowledge of regulatory guidelines (e.g., ICH-GCP) and relevant clinical R&D concepts is required.
• Experience working with cross-functional stakeholders, vendor management oversight, and project management skills are preferred.