Senior Principal Statistical Programmer - Remote

Tevapharm; Almería; Remote; EUR 85,000 - 110,000; Full time

Benefits offered by this job

Remote work

Job summary

Cytel seeks a Senior/Principal Statistical Programmer (SAS + R) to work fully embedded with a pharmaceutical client. You will implement reporting and analysis activities for Sponsor trials, leveraging CDISC standards and FDA/ICH guidelines.

The role requires independent work, senior technical leadership, and collaboration with CROs and internal teams. Remote work from Spain is supported in a globally connected program.

Qualifications

• 7+ years of experience as a Statistical Programmer in Biotech/Pharma Clinical Development Biometrics Team or similar.
• Exceptional SAS programming skills in clinical development environments.

Responsibilities

• Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml for multiple studies.
• Develop SAS programs to create datasets, listings, tables and complex graphs.
• Deliver high-quality programming results with SAS and/or R for clinical programs.
• Oversee CRO programming deliverables to meet timelines.
• Support clinical study reports, regulatory submissions and DSURs.

Skills

SAS

R

CDISC (SDTM/ADaM)

FDA/ICH regulations

Leadership

Communication

Education

Bachelor's degree in Computer Science or Data Science or Mathematics or Statistics

Tools

SAS

R

Job description

Cytel seeks a Senior/Principal Statistical Programmer (SAS + R) to work fully embedded with a pharmaceutical client. You will implement reporting and analysis activities for Sponsor trials, leveraging CDISC standards and FDA/ICH guidelines.

The role requires independent work, senior technical leadership, and collaboration with CROs and internal teams. Remote work from Spain is supported in a globally connected program.