Senior Executive Recruiter — High-Impact, Sandton

Placements24; Gauteng; A distancia; ZAR 900.000 - 1.500.000; Jornada completa

Descripción de la vacante

Cytel is seeking a Senior/Principal Statistical Programmer to work remotely on sponsor-driven clinical development programs, delivering high-quality programming support across SDTM/ADaM outputs and regulatory deliverables.

You will independently manage complex analyses, generate datasets and tables, and collaborate with statisticians and CROs to ensure timely, accurate results for multiple studies in a global setting.

Formación

• Senior/Principal Statistical Programmer with SAS and R experience.
• Experience delivering SDTM/ADaM datasets and regulatory deliverables.
• Clinical trial programming experience across multiple therapeutic areas.

Responsabilidades

• Generate SDTM/ADaM specifications, datasets, and define.xml.
• Develop SAS programs for listings, tables, and graphs.
• Coordinate with statisticians and CROs to ensure data of high quality.

Conocimientos

SAS

R

Clinical trials

Herramientas

SDTM

ADaM

Descripción del empleo

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Senior/Principal Statistical Programmer SAS + R (Remote)

**Sponsor-dedicated:**
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 individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.
**Position Overview:**
This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials.
**As a Principal Statistical Programmer, your responsibilities will include:**
+ Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies
+ Develop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs
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