SR. CLINICAL SAS PROGRAMMER

The Principal Statistical Programmer is responsible for providing leadership and hands-on support in the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. The individual will work closely with the Associate Director, Director, and Statistical Programmers to build internal programming tools. This individual, working closely with the study team, will be responsible for review and acceptance of contract research organizatio

HCL Technologies Limited Key Responsibilities: * Create advanced SAS macros, templates, and utilities for efficient data processing * Act as the primary programming point of contact for biostatisticians and study teams * Perform peer review of code and documentation for accuracy and traceability * Review CRF (Case Report Form) annotations and data specifications. * Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines. Skill Requirements: * Extensive programming experi

Position Purpose: The Senior Programmer for Data Validation supports cross-functional teams such as Statistics, Data Management and Standards by overseeing and ensuring the quality of clinical data build and programming activities across in-house, hybrid, and vendor-supported studies. The role focuses on governance, review, and validation of deliverables to ensure alignment with CSL standards, regulatory requirements, and industry best practices. The incumbent applies strong expertise in CDASH a

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we?re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director, Programming (Macros & Automation)? The job is in our Waltham MA, King of Prussia PA or Glattbrugg Sw