Senior Statistical Programmer - Remote & Global Projects

Meeveem Limited

Maidenhead

On-site

GBP 90,000 - 120,000

Full time

14 days+

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Job summary

Fortrea is seeking a Principal Statistical Programmer to lead programming activities for complex clinical trials in a sponsor-dedicated Flexible Solutions unit. The role involves SDTM/ADaM development, senior review, and cross‑functional collaboration across Clinical, Medical Writing and Safety teams.

You will mentor junior staff, contribute to publication support and submission activities, and ensure high-quality, timely outputs within a global CRO environment.

Qualifications

  • Degree or equivalent with strong background in statistics or science.
  • Minimum 5 years of experience in statistical programming for clinical trials.
  • Expertise in SDTM/ADaM and CDISC standards; experience with define.xml and submission prep.

Responsibilities

  • Plan, execute and oversee programming activities for a study, including resourcing and timelines.
  • Oversee SDTM, ADaM and TLF development and perform senior review of outputs.
  • Liaise with sponsor departments for programming needs supporting publications and analyses.
  • Support/oversee submission activities, especially in late phase teams.
  • Ensure efficiency and quality, with proper tools and macros setup.
  • Mentor junior team members in best practices and adherence to standards.

Skills

Statistical programming
SDTM/ADaM
SAS programming
SAS macros
CDISC standards
Mentoring
Cross-functional collaboration
English communication

Education

Degree in mathematics, life sciences, statistics, computer sciences

Tools

SAS

Job description

Fortrea is seeking a Principal Statistical Programmer to lead programming activities for complex clinical trials in a sponsor-dedicated Flexible Solutions unit. The role involves SDTM/ADaM development, senior review, and cross‑functional collaboration across Clinical, Medical Writing and Safety teams.

You will mentor junior staff, contribute to publication support and submission activities, and ensure high-quality, timely outputs within a global CRO environment.

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