Lead / Principal Clinical SAS Programmer (5+ Years)

Job Description

The Lead/Principal Clinical SAS Programmer oversees programming strategy, ensures compliance with regulatory standards, and leads teams across multiple clinical studies.

Key Responsibilities

• Lead end-to-end programming activities for studies

• Define programming standards and workflows

• Review and approve SAS programs and outputs

• Mentor junior programmers and conduct trainings

• Support regulatory submissions and audits

• Act as primary liaison with Biostatistics and sponsors

Skills & Requirements

• 5+ years of Clinical SAS experience

• Expert knowledge of CDISC standards and regulatory submissions

• Leadership and project management skills

• Strong client-facing and problem-solving abilities