Principal Statistical Programmer

Cytel Inc. seeks a Senior/Principal Statistical Programmer SAS + R for remote work within our sponsor-dedicated team. You will lead statistical programming for multiple clinical trials, implement SDTM/ADaM, and oversee CROs to ensure timely, high-quality data deliverables and regulatory submissions. You will work independently with minimal supervision,...

JOB DESCRIPTION Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where...

Cytel Inc. seeks a Senior/Principal Statistical Programmer SAS + R for remote work within our sponsor-dedicated team. You will lead statistical programming for multiple clinical trials, implement SDTM/ADaM, and oversee CROs to ensure timely, high-quality data deliverables and regulatory submissions. You will work independently with minimal supervision,...

Cytel is seeking a Principal Statistical Programmer embedded with a leading pharmaceutical client. The role requires independent work, advanced SAS programming, and strong CDISC expertise to deliver datasets, tables, and listings for regulatory submissions. You will collaborate with CROs and internal teams, maintain standards, and contribute to study reports...

Job Overview: As a Principal Statistical Programmer you will provide advanced technical expertise to develop process methodology for the department to meet internal and external clients’ needs, across complex projects and studies. This involves planning and coordinating the development of integrated programming solutions, serving the full spectrum of...

Overview Work as a principal programmer across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...

Overview Work as a principal programmer across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area; producing,...

IQVIA is seeking a Principal Statistical Programmer to provide advanced technical leadership across complex studies. You will plan and coordinate integrated programming solutions, develop specifications, and act as internal consultant for client requirements. You will lead programming quality controls, mentor SP team members, and collaborate with...

As a Principal Programmer within our FSP team, you will be working embedded within the sponsors team, to support market access, value and pricin Responsibilities * ties Develop and validate ADaM and TLF’s for Health Technical Assessment (HTA) & Health Economics and Outcomes Research * (HEOR)Generate analysis to be used primarily for HTA, HEOR submissions...