Senior Sap Analytics Architect (Datasphere & Sac) – Hybrid

Puig Deutschland Gmbh; Barcelona; Remote; EUR 90,000 - 120,000; Full time

Job summary

Cytel is seeking a Principal Statistical Programmer to work remotely with a leading pharmaceutical client. You will lead programming activities across SDTM/ADaM outputs, develop SAS and R programs, and ensure high-quality data deliverables on multiple studies.

In this role you will oversee CRO programmers, collaborate with statisticians, and support the biostatistics team in delivering accurate summaries and figures while maintaining timelines and standards.

Qualifications

• Extensive experience as a senior statistical programmer in clinical development.

Responsibilities

• Generate SDTM, ADaM specs, datasets, and define.xml for multiple studies.
• Develop SAS programs to create datasets, listings, tables, and graphs.
• Deliver SAS/R programs for clinical development programs with high quality.
• Oversee CRO deliverables for multiple studies to meet timelines.
• Provide technical support to team members.

Skills

SAS

R

SDTM

ADaM

CDISC

CRO oversight

Clinical programming

Job description

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
• Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs
• Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines
• Support