Tech Stack

Description

You will lead clinical programming strategy across multiple studies, manage internal and external programmers, establish standards, and ensure high-quality deliverables for regulatory submissions. This hybrid role is based in Waltham, MA.

Requirements

• Strong expertise in SAS and/or R
• Deep knowledge of CDISC standards
• Experience supporting regulatory submissions
• Strategic and technical leadership experience
• Experience managing internal and external resources

Responsibilities

• Lead programming strategy across multiple clinical studies and development programs
• Oversee and manage internal programmers and external vendors/CRO partners
• Establish and maintain programming standards, processes, and best practices
• Support planning, timelines, and resourcing for all programming activities
• Drive adoption of modern programming tools and standards