Senior Statistical Programmer: Drive Global Clinical Data

TFS HealthScience; Stockholms kommun; On-site; SEK 700,000 - 950,000; Full time

Job summary

TFS HealthScience is seeking a Senior Statistical Programmer to provide SAS programming expertise across global clinical studies. You will work with cross-functional teams to review data, support analyses, and ensure high-quality deliverables for regulatory submissions.

Ideal candidates have a strong SAS background, CDISC SDTM/ADaM experience, and familiarity with TLFs. This is a role within our SRS/FSP team, dedicated to one sponsor, with opportunities for growth in a global CRO.

Qualifications

• Bachelor's or Master's degree in Statistics, Biostatistics, Mathematics, Computer Science, Life Sciences, or a related field.
• Experience in Statistical Programming within pharmaceutical, biotechnology, or CRO industry.
• Strong SAS programming skills.
• Experience with CDISC standards (SDTM/ADaM).
• Experience producing Tables, Listings, and Figures (TLFs).
• Solid understanding of clinical trial methodology, ICH-GCP, and regulatory requirements.
• Ability to review and interpret clinical data and statistical outputs.
• Experience working with external vendors or CRO partners is highly desirable.

Responsibilities

• Develop, validate, and maintain SAS programs for clinical trial reporting and analysis.
• Generate and review SDTM and ADaM datasets in accordance with CDISC standards.
• Produce and validate Tables, Listings, and Figures (TLFs) for study reports and regulatory submissions.
• Review, assess, and interpret clinical study data to support study teams.
• Evaluate protocol deviations and assess their impact on study outcomes.
• Review statistical analyses and deliverables from external service providers.
• Collaborate with Biostatistics, Clinical Operations, and Data Management teams to ensure high quality study execution.
• Contribute to data review activities and support the development of analysis specifications.
• Support regulatory submissions and ensure statistical deliverables are inspection-ready.
• Drive continuous improvement of programming standards and automation.

Skills

Strong communication

Cross-functional collaboration

Adaptability

Education

Bachelor's or Master's degree in Statistics/Biostatistics/Mathematics/Computer Science/Life Sciences

Tools

SAS

SDTM/ADaM CDISC standards

TLFs (Tables, Listings, Figures)

R programming

Job description

TFS HealthScience is seeking a Senior Statistical Programmer to provide SAS programming expertise across global clinical studies. You will work with cross-functional teams to review data, support analyses, and ensure high-quality deliverables for regulatory submissions.

Ideal candidates have a strong SAS background, CDISC SDTM/ADaM experience, and familiarity with TLFs. This is a role within our SRS/FSP team, dedicated to one sponsor, with opportunities for growth in a global CRO.