Know ATS Score
CV/Résumé Score
  • Expertini Resume Scoring: Our Semantic Matching Algorithm evaluates your CV/Résumé before you apply for this job role: Senior Statistical Programmer.
Spain Jobs Expertini

Urgent! Senior Statistical Programmer Job Opening In Madrid – Now Hiring Meet Life Sciences

Senior Statistical Programmer



Job description

We are seeking an experienced Senior or Principal Statistical Programmer to join a Functional Service Provider (FSP) team , supporting a leading global pharmaceutical company.

This role provides an opportunity to work on innovative clinical trials in a dynamic and collaborative environment, contributing to the development of life-changing medicines.
About the Role:
The Senior/Principal Statistical Programmer (FSP) will be responsible for developing, validating, and maintaining SAS programs for the analysis and reporting of clinical trial data.
Location: Remote
Employment Type: Full-time
Key Responsibilities: Develop, validate, and maintain SAS programs for the analysis and reporting of clinical trial data.
Generate tables, listings, figures (TLFs), and analysis datasets (ADaM, SDTM) in accordance with CDISC standards.
Collaborate with biostatisticians, data managers, and clinical teams to ensure accurate and efficient data analysis.
Perform quality control (QC) checks to ensure regulatory compliance and adherence to industry standards.
Contribute to programming strategies, supporting regulatory submissions and responses.
Guide and mentor junior programmers, fostering knowledge-sharing within the team.
Ensure compliance with sponsor standards, guidelines, and processes while working within the FSP model.
Key Requirements: BSc, MSc, or equivalent experience in Statistics, Computer Science, Mathematics, Life Sciences, or a related field.
5+ years (Senior) / 8+ years (Principal) of statistical programming experience in a clinical trial setting (CRO, pharma, or biotech).
Strong proficiency in SAS programming (Base, Macro, SQL, Graph, and STAT) .
Experience in R Programming is preferable but not required.
Experience with CDISC standards (SDTM, ADaM) and regulatory submission requirements (e.g., FDA, EMA).
Familiarity with statistical methodologies and clinical trial design.
Ability to work effectively within a global team and manage multiple priorities.
Excellent problem-solving and communication skills.
What We Offer: Competitive salary and benefits package.
Opportunity to work on global clinical trials in collaboration with a leading pharmaceutical company.
Professional development and career growth opportunities.
A flexible and supportive work environment (remote/hybrid options).

#J-18808-Ljbffr


Required Skill Profession

Other General



Your Complete Job Search Toolkit

✨ Smart • Intelligent • Private • Secure

Start Using Our Tools

Join thousands of professionals who've advanced their careers with our platform

Rate or Report This Job
If you feel this job is inaccurate or spam kindly report to us using below form.
Please Note: This is NOT a job application form.


    Unlock Your Senior Statistical Potential: Insight & Career Growth Guide