Senior Principal Statistical Programmer - SAS + R (Remote)

Eurecat; Santiago de Compostela; Remote; EUR 70,000 - 100,000; Full time

Benefits offered by this job

Remote work

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer for a remote role. You will work on one or more global pharmaceutical clients, delivering SAS and R based analyses, SDTM/ADaM specifications, and high-quality data outputs with CRO oversight.

The role involves collaboration with biostatistics and programming leaders, preparing regulatory submissions and study reports while adhering to GCP and FDA guidelines. Remote work available globally.

Qualifications

• Extensive SAS and R programming experience in clinical development.
• Proven work with SDTM/ADaM specifications and data listings.
• Experience overseeing CROs and ensuring project timelines.

Responsibilities

• Generate SDTM and ADaM specifications, datasets, and define.xml files for multiple studies.
• Develop SAS programs to produce datasets, listings, tables, and graphs.
• Deliver high-quality SAS/R outputs for clinical development programs.
• Oversee CRO deliverables to ensure accuracy and timeliness.
• Support preparation of SCRs, regulatory submissions, and publications.
• Ensure compliance with GCP and regulatory guidelines for submissions.

Skills

SAS programming

R programming

SDTM/ADaM

Clinical trials

CRO oversight

Tools

SAS

R

Job description

Cytel is seeking a Senior/Principal Statistical Programmer for a remote role. You will work on one or more global pharmaceutical clients, delivering SAS and R based analyses, SDTM/ADaM specifications, and high-quality data outputs with CRO oversight.

The role involves collaboration with biostatistics and programming leaders, preparing regulatory submissions and study reports while adhering to GCP and FDA guidelines. Remote work available globally.