Tech Stack

Description

You will lead statistical programming activities for clinical trials, manage programmers and CROs, and collaborate cross-functionally to ensure high-quality data deliverables and regulatory compliance.

Requirements

• Master's degree in Statistics, Biostatistics, or related field
• 10+ years of clinical trial programming experience in biotech/pharma
• Advanced SAS and R programming skills
• In-depth knowledge of CDISC standards (SDTM, ADaM)
• Experience managing CROs and data vendors

Responsibilities

• Serve as lead statistical programmer on clinical studies
• Oversee programming vendors, review and validate datasets and TFLs
• Collaborate with cross-functional teams for timely data deliverables
• Develop and implement data review tools and programming standards
• Build and mentor a team of programmers