Tech Stack

Description

You will lead statistical programming activities within the Biometrics group, overseeing clinical programming deliverables, ensuring quality and compliance, supporting regulatory submissions, and mentoring a team of programmers. This role offers the security of a global CRO with the opportunity to work directly for a single sponsor.

Requirements

• Strong expertise in SAS and/or R
• Deep knowledge of CDISC standards
• Experience with oncology clinical trials
• Excellent leadership skills
• Proven experience managing statistical programming activities in a clinical research environment

Responsibilities

• Lead and mentor a team of statistical programmers
• Oversee internal and vendor/CRO programming deliverables for timelines and quality
• Establish and maintain programming standards, documentation, and best practices
• Support planning, resourcing, and prioritization for programming activities across multiple studies
• Oversee development and validation of SDTM and ADaM datasets per CDISC standards and oncology study requirements