Avania are hiring - Statistical Programmer
About the role
We are looking for a Statistical Programmer to own the statistical programming process across clinical studies. You will create analysis datasets and program tables, listings, and figures (TLFs), working in a validated, highly regulated environment.
This role is open to candidates in Spain, the Netherlands, and the UK. You will support approximately three to five studies at a time across a variety of therapeutic areas, depending on each study’s stage and needs.
What you’ll do
- Create and maintain analysis datasets for clinical studies.
- Program tables, listings, and figures (TLFs), primarily using SAS.
- Interpret study protocols and translate analysis requirements into accurate programming outputs.
- Follow validation, cross-checking, and quality standards appropriate to a highly regulated environment.
- Work closely with biostatisticians and data managers, with occasional collaboration with clinical research associates.
- Contribute across multiple studies and therapeutic areas simultaneously.
- Support CDISC standardization when required by the client or project.
Candidates who offer a combination of the skills, knowledge and experience listed below are encouraged to apply to our Statistical Programmer role . With our continued growth we are hiring talent to join us on our journey and grow with us.
What we’re looking for
- Hands-on SAS programming experience.
- Some experience or exposure— including through an internship—to statistical programming in a CRO, sponsor, or similar regulated clinical research setting.
- Familiarity with validated programming environments, quality checks, and regulated standards.
- The ability to understand study protocols and programming requirements.
- Clear communication skills and the ability to collaborate effectively with biostatistics and data management colleagues.
- Strong organization and attention to detail when supporting multiple studies.
Nice to have
- Exp
📌 Statistical Programmer (España)
🏢 Avania
📍 España