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Senior Statistical Programmer (m/w/d) - Fully homebased/remote

TN United Kingdom

London

Remote

GBP 45,000 - 75,000

Full time

Today
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Job summary

An established industry player is seeking a Senior Statistical Programmer to join their innovative team. This fully remote role offers the chance to develop clinical study report materials using SAS programming for regulatory submissions. With a focus on quality control and data analysis, you'll collaborate with statisticians and clinical teams on global projects, contributing to advancements in human health. Ideal candidates will have extensive experience in the healthcare sector and a strong educational background in biostatistics or related fields. Join a fast-paced, collaborative environment that values development and mentoring opportunities.

Qualifications

  • 5+ years of experience as a Statistical Programmer in CRO/Pharma.
  • Expertise in ADaM/SDTM/TLFs and SAS programming.

Responsibilities

  • Develop clinical study report materials using SAS programming.
  • Collaborate with statisticians and clinical teams on global projects.

Skills

SAS Programming
Data Import
Quality Control
Statistical Analysis
Attention to Detail
Leadership Potential
Communication Skills

Education

Master’s or Bachelor’s degree in Biostatistics
Degree in Statistics
Degree in Mathematics
Degree in Computer Science

Job description

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Senior Statistical Programmer (m/w/d) - Fully homebased/remote, London
Client:

IQVIA

Location:

London, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Reference:

a630f467b321

Job Views:

8

Posted:

26.04.2025

Expiry Date:

10.06.2025

Job Description:

IQVIA is seeking experienced statistical programmers to develop clinical study report materials using SAS programming language for regulatory submissions. Responsibilities include data import, quality control, programming SDTM and ADaM datasets, creating analysis tables, validating outputs, and collaborating with statisticians and clinical teams. The role offers the opportunity to work on global projects in a fast-paced, collaborative environment with development and mentoring opportunities.

Qualifications:

  • Master’s or Bachelor’s degree in Biostatistics, Statistics, Mathematics, or Computer Science
  • At least 5 years of experience as a Statistical Programmer in CRO/Pharma, with expertise in ADaM/SDTM/TLFs

Key skills include SAS programming in healthcare industries, knowledge of statistics, attention to detail, understanding of GCP and ICH guidelines, leadership potential, and strong communication skills. This role is remote and does not qualify for UK visa sponsorship. IQVIA is a global leader in analytics and clinical research, committed to advancing human health through innovative science and data.

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