As a Senior Statistical Programmer, you will be working embedded within the sponsor FSP team, delivering SAS programming in line with CDISC standards (SDTM and ADa M).

The role focuses on vendor oversight and end-to-end project coordination to ensure high-quality, on-time clinical data deliverables.

Responsibilities Program, QC, and maintain SDTM and ADa M datasets in SAS in accordance with CDISC standards Coordinate programming deliverables, timelines, and dependencies across sponsor stakeholders and external vendors Provide oversight of vendor programming activities, including review of specifications, deliverables, and issue resolution Support CDISC-compliant submission deliverables (e.g., define.xml support and dataset-level metadata) in collaboration with internal teams and vendors Lead programming workstreams by planning, tracking, and communicating status/risks for SDTM and ADa M deliverables Perform SDTM and ADa M mapping/derivations and ensure traceability from source to analysis datasets Apply and maintain study standards for SDTM and ADa M implementation (structures, variables, controlled terminology) across internal and vendor outputs Drive issue management for SDTM/ADa M deliverables (e.g., review findings, validation queries, and remediation) through to closure Perform senior review and QC of SDTM and ADa M datasets and associated documentation, including vendor deliverables Create, QC, and maintain SDTM and ADa M dataset specifications and ensure alignment with study standards and vendor outputs Qualifications Educated to BSc or above within Computer Science,



Mathematics or a Science related discipline SAS & R Programming experience within the Pharmaceutical or CRO industry Knowledge of SDTM and ADa M CDISC standards Why Join Us Remote working and flexible working hours Career development, mentorship, and continuous learning Supportive, friendly, and collaborative culture Making a Positive Impact: As a B-Corp organization, we are committed to sustainability, solid responsibility and strong ethical governance through our ESG initiatives About Phastar Phastar is an award-winning biometrics and data science CRO, trusted by pharma, biotech, and medical device companies worldwide.

With a general team of data specialists, we bring expertise, precision, and pace to every trial, because behind every data point is a patient waiting for treatment.

We transform complex data into clear, actionable intelligence, helping accelerate drug development, and bring life-changing therapies to patients faster.

Awards & Recognition SCRIP – Best Contract Research Organization, Specialist Provider Citeline – 2025 Award Winner Fierce CRO Awards – Recognized Industry Leader Phastar is committed to the principles and practices of equal opportunities and to encourage the establishment of a diverse workforce.

It is our policy to employ individuals on the basis of their suitability for the work to be performed and their potential for development, regardless of age, sex, race, color, nationality, ethnic or national origin, disability, marital status, pregnancy or maternity, sexual orientation, gender reassignment, religion, or belief.

This includes creating a culture that fully reflects our commitment to equal opportunities for all. #J-18808-Ljbffr

📌 Senior statistical programmer (España)
🏢 PHASTAR
📍 España