Principal Statistical Programmer (Remote) - SAS/R, CDISC

Experis España; Alicante; Remote; EUR 70,000 - 110,000; Full time

Job summary

Experis España is seeking a Senior/Principal Statistical Programmer (SAS + R) for a remote role. You will be dedicated to a global pharmaceutical client and work within Cytel's FSP Services framework, overseeing CRO programmers to ensure data summaries are delivered with autonomy and high quality.

The ideal candidate has extensive experience in clinical development programs, develops SDTM/ADaM specifications, and supports regulatory submissions.

Qualifications

• Senior-level statistical programmer with experience in clinical development.
• Ability to develop SAS programs that generate datasets, tables, and listings.
• Experience coordinating CRO programmers to ensure timely, high-quality deliverables.
• Familiarity with regulatory submissions and reporting for clinical trials.

Responsibilities

• Generate SDTM, ADaM specifications, datasets, and define.xml for multiple studies.
• Develop SAS programs to create datasets, listings, tables, and graphs.
• Deliver high-quality programming outputs and validate SAS and/or R programs.
• Oversee CRO's statistical programming deliverables across studies to meet timelines.
• Support preparation of clinical study reports, regulatory submissions, and publications.
• Ensure adherence to FDA regulations and GCP for electronic submissions.
• Contribute to standards for programming tools, outputs, and macros.
• Assist in CRF development, edit check specs, and data validation plans.
• Provide review of programming deliverables for quality assurance.

Skills

SAS programming

R programming

Clinical development programs

CRO oversight

Data analysis

Tools

SAS

R

Job description

Experis España is seeking a Senior/Principal Statistical Programmer (SAS + R) for a remote role. You will be dedicated to a global pharmaceutical client and work within Cytel's FSP Services framework, overseeing CRO programmers to ensure data summaries are delivered with autonomy and high quality.

The ideal candidate has extensive experience in clinical development programs, develops SDTM/ADaM specifications, and supports regulatory submissions.