SDTM/Data Management SAS Programmer | Clinical Trials

Veramed

England

On-site

GBP 45,000 - 65,000

Full time

14 days+
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Job summary

Veramed is seeking a Data Management Programmer to join a sponsor-dedicated team, working as a fully integrated member of a global Data Management Programming function. The role focuses on generating Data Management listings from raw clinical trial data using SAS, with an opportunity to gain exposure to SDTM programming over time.

You will generate listings, draft Define.xml and SDRG documentation, and support milestones such as Dry Runs and Interim Analyses while ensuring adherence to sponsor

Qualifications

  • Proven SAS programming experience in clinical research.
  • Knowledge of CDISC SDTM standards (v3.3 and/or v3.4).
  • Experience developing or QC'ing SDTM datasets.
  • Familiarity with Pinnacle 21 or similar validation tools.
  • Excellent communication and stakeholder management skills.

Responsibilities

  • Generate Data Management listings and support protocol deviation reporting.
  • Develop or quality control SDTM datasets for individual studies and pooled analyses.
  • Produce and review Define.xml and SDRG documentation.
  • Support key clinical milestones including Dry Runs, Interim Analyses, IDMC reviews, DSURs and Final Analyses.
  • Ensure all deliverables comply with sponsor SOPs, processes and quality standards.
  • Collaborate with cross-functional teams and communicate project risks or issues as needed.

Skills

SAS programming
CDISC SDTM standards
SDTM dataset development
Pinnacle 21 validation
Communication & stakeholder management

Tools

Pinnacle 21

Job description

Veramed is seeking a Data Management Programmer to join a sponsor-dedicated team, working as a fully integrated member of a global Data Management Programming function. The role focuses on generating Data Management listings from raw clinical trial data using SAS, with an opportunity to gain exposure to SDTM programming over time.

You will generate listings, draft Define.xml and SDRG documentation, and support milestones such as Dry Runs and Interim Analyses while ensuring adherence to sponsor

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