Senior Statistical Programmer (Biopharmaceutical, Hellerup)

Job summary

This role involves contributing to the development and improvement of SDTM programming within clinical trials, focusing on statistical programming to support data analysis and reporting. The position is part of a global team dedicated to advancing innovative therapies in the biopharmaceutical sector.

Qualifications

• Relevant academic degree, preferably a Master’s or PhD, in statistics, mathematics, computer science, engineering, life sciences, or a related field.
• Minimum of 5 years of experience in clinical trials within the pharmaceutical or biotechnology industry, utilizing SAS and/or R.
• Experience in developing and validating SDTM datasets, with knowledge of CDISC SDTM standards.

Responsibilities

• Participate in the SDTM programming group, aiding in the planning and development of SDTM deliverables.
• Conduct statistical programming activities to support clinical data analysis and reporting.
• Collaborate with international colleagues in a dynamic environment.

Skills

• Strong analytical skills and attention to detail, ensuring high-quality deliverables.
• Ability to communicate effectively with both technical and non-technical stakeholders.
• Familiarity with Python and understanding of metadata-driven programming approaches.

Education

• Advanced degree (Master’s or PhD) in a relevant field preferred.

Tools

• Proficient in SAS and/or R for statistical programming.
• Knowledge of regulatory submission requirements including CDISC standards.