Enginyer/A Sènior - Instal·Lacions Industrials

Etalentum; Oña; Remote; EUR 70,000 - 110,000; Full time

Job summary

Etalentum is seeking a Senior/Principal Statistical Programmer SAS + R for a fully remote role, sponsored within a pharmaceutical client with Cytel support. The role focuses on delivering SDTM/ADaM specifications, datasets, and regulatory-grade outputs for multiple studies.

The Senior/Principal Programmer leads SAS/R development, ensures data quality, oversees CRO deliverables, and contributes to study reports and regulatory submissions while maintaining FDA/GCP compliance.

Qualifications

• Extensive experience in statistical programming for clinical trials.
• Expertise in SAS and R programming.
• Knowledge of CDISC SDTM/ADaM standards.

Responsibilities

• Develop SDTM/ADaM datasets and define.xml for studies.
• Write SAS and R programs for listings and tables.
• Oversee CRO programmers and ensure timelines.
• Prepare clinical study reports, submissions, and regulatory documents.
• Ensure compliance with FDA/ICH guidelines.

Skills

Statistical programming

Clinical trials

Team collaboration

Tools

SAS

R

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 the preparation of clinical study reports, regulatory submissions, publications, annual DSUR, and exploratory analyses
• Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions.
• Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros
• Participate in the development of CRFs, edit check specifications, and data validation plans
• Provide review