Senior Principal Statistical Programmer (SAS + R) Remote

Radical Games Sl; Alicante; Remote; EUR 65,000 - 95,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer SAS + R (Remote) to work embedded with a pharmaceutical client. The Principal Programmer works independently with minimal supervision and provides expert technical support to the team, overseeing CRO programmers to ensure data summaries are delivered to a high quality.

As a Principal Statistical Programmer, you will implement all reporting and analysis activities for Sponsor clinical trials, develop SDTM/ADaM artifacts, and ensure

Qualifications

• Principal Statistical Programmer works independently with limited supervision.
• Responsible for implementing reporting and analysis activities for Sponsor clinical trials.

Responsibilities

• Generate SDTM, ADaM specs, datasets, reviewer’s guide and define.xml for studies
• Develop SAS programs to generate datasets, complex listings, tables and graphs
• Deliver high-quality statistical programming results including SAS and/or R programs
• Oversee CRO's statistical programming deliverables to meet timelines
• Support preparation of clinical study reports, regulatory submissions and DSUR
• Understand FDA regulations for reporting clinical trial data
• Contribute to standards for programming tools, outputs, and macros
• Participate in development of CRFs, edit checks, and data validation plans
• Provide review of programming outputs and quality checks

Skills

SAS programming

R programming

Independent worker

Regulatory compliance

Tools

SAS

R

CDISC standards

Job description

Cytel is seeking a Senior/Principal Statistical Programmer SAS + R (Remote) to work embedded with a pharmaceutical client. The Principal Programmer works independently with minimal supervision and provides expert technical support to the team, overseeing CRO programmers to ensure data summaries are delivered to a high quality.

As a Principal Statistical Programmer, you will implement all reporting and analysis activities for Sponsor clinical trials, develop SDTM/ADaM artifacts, and ensure