Senior Principal Statistical Programmer - SAS + R (Remote)

Between Technology; Madrid; Remote; EUR 70,000 - 90,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer (Remote) to join a sponsor-dedicated program embedded with a pharmaceutical client. You will implement reporting and analysis activities across trials, ensuring high-quality outputs and adherence to FDA guidelines.

Applicants should bring extensive SAS and R programming experience in clinical development, with ability to oversee CRO workstreams and collaborate with statisticians to deliver robust results for regulatory submissions.

Qualifications

• Extensive experience in statistical programming for clinical trials.
• Strong knowledge of SDTM/ADaM data structures and specifications.
• Experience coordinating CRO programming deliverables and timelines.
• Familiarity with FDA/ICH guidelines and electronic submissions.

Responsibilities

• Generate SDTM and ADaM specifications, datasets, reviewer’s guides and define.xml for multiple studies.
• Develop SAS programs to create datasets, listings, tables, and graphs.
• Deliver high-quality programming outputs and maintain SAS and/or R programs for development programs.
• Oversee CRO programmers to ensure timely, accurate deliverables for studies and submissions.
• Support generation of clinical study reports, regulatory submissions, and exploratory analyses.

Skills

SAS

R

SDTM

ADaM

Clinical trials

CRO oversight

Tools

SAS (software)

R (software)

Job description

Cytel is seeking a Senior/Principal Statistical Programmer (Remote) to join a sponsor-dedicated program embedded with a pharmaceutical client. You will implement reporting and analysis activities across trials, ensuring high-quality outputs and adherence to FDA guidelines.

Applicants should bring extensive SAS and R programming experience in clinical development, with ability to oversee CRO workstreams and collaborate with statisticians to deliver robust results for regulatory submissions.