SAS Statistical Programmer: Real-World Evidence & Clinical Data

LEO Pharma; Ballerup; On-site; DKK 700,000 - 900,000; Full time

Job summary

LEO Pharma seeks a SAS Statistical Programmer to transform clinical and real-world data into robust evidence across development, publications, and market access. You will work on Phase 2b–4 trials and non-interventional studies, delivering high-quality SAS outputs and contributing to publications and HTA discussions.

Required MSc/PhD in STEM, strong SAS skills, CDISC experience (ADaM/SDTM), and comfort with R.

Qualifications

• MSc or PhD in STEM with solid quantitative background.
• Strong SAS programming skills and ability to produce high-quality outputs.
• Experience with clinical/healthcare data and CDISC standards (ADaM/SDTM).

Responsibilities

• Program, quality control, validate, and document datasets, tables, figures, and listings using SAS.
• Conduct statistical analyses for publication-related requests and abstracts.
• Support subgroup Analyses for pricing and reimbursement negotiations.
• Contribute statistical thinking to HTA and payer-related deliverables.
• Assist analyses for meta-analyses and indirect treatment comparisons.

Skills

SAS programming

Statistical analysis

CDISC (ADaM/SDTM)

R familiarity

Clinical data experience

Education

MSc or PhD in STEM

Tools

R

Job description

LEO Pharma seeks a SAS Statistical Programmer to transform clinical and real-world data into robust evidence across development, publications, and market access. You will work on Phase 2b–4 trials and non-interventional studies, delivering high-quality SAS outputs and contributing to publications and HTA discussions.

Required MSc/PhD in STEM, strong SAS skills, CDISC experience (ADaM/SDTM), and comfort with R.