Rabi Solutions
Senior Statistical Programmer – Clinical SAS
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🚨 Hiring | Senior Clinical SAS Programmer – Clinical Trials
🌍 Candidates based anywhere in Europe are welcome to apply.
We are looking for an experienced Senior Clinical SAS Programmer to support clinical trial statistical programming activities across various stages of clinical development.
🔹 Key Responsibilities
- Develop, validate, and maintain SAS programs for clinical trial data analysis and reporting
- Program and validate SDTM and ADaM datasets in accordance with CDISC standards
- Develop Tables, Listings, and Figures (TLFs) for clinical studies
- Work with raw clinical data and transform it into analysis-ready datasets
- Develop and maintain SAS macros, DATA step and PROC SQL programs
- Perform programming QC and independent validation of clinical outputs
- Support clinical study reports and regulatory submission deliverables
- Review programming specifications and ensure deliverables meet quality and regulatory requirements
- Collaborate closely with Biostatisticians, Statistical Programmers, Data Managers, and Clinical teams
- Support programming activities across different phases of clinical trials
- Ensure compliance with applicable SOPs, CDISC standards, GCP and regulatory requirements
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🔹 Required Skills & Experience
✅ 6+ years of experience in Clinical SAS / Statistical Programming
✅ Strong hands-on experience with Base SAS
✅ Strong knowledge of SAS Macro, DATA Step, PROC SQL and SAS procedures
✅ Strong experience with SDTM and ADaM
✅ Hands-on experience developing TLFs
✅ Experience working with clinical trial datasets
✅ Experience with clinical study reporting and/or regulatory submissions
✅ Good understanding of clinical trial processes and statistical programming
✅ Experience with programming validation and QC
✅ Strong analytical, problem-solving and communication skills
✅ Ability to work effectively with international and cross-functional teams
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🔹 Preferred Skills
- Experience working with CRO, Pharmaceutical or Biotechnology organizations
- Experience supporting FDA / EMA regulatory submissions
- Knowledge of Define-XML and CDISC implementation
- Experience in one or more therapeutic areas
- Knowledge of R programming is an advantage
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