Full Time

Senior Clinical Programmers (EDC or SAS)

Elixir Associates
Contract
Mid-Senior level
Research Services, Pharmaceutical Manufacturing, and Biotechnology Research
United States
???* / year

Job Description

Fully Remote | Oncology | AI & Clinical Data Innovation


We're partnering with an innovative life sciences organisation at the forefront of oncology research, advanced data technology and artificial intelligence, seeking two experienced programmers to join its growing clinical data function.


These opportunities offer meaningful technical challenges, exposure to cutting-edge clinical research and a genuinely supportive working environment.


Senior SAS / Clinical Programmer

  • Strong hands-on SAS programming, including macros, clinical datasets and reporting.
  • Excellent knowledge of CDISC, SDTM and CDASH standards.
  • Clinical data integration, validation and data review experience.
  • Medidata Rave experience (essential); Medrio advantageous.
  • Ideally, early-phase oncology experience.


Senior EDC / Database Programmer

  • 5+ years of hands-on Medidata Rave experience, ideally certified.
  • Expertise in EDC study builds, eCRFs, complex edit checks and database validation.
  • Experience with clinical database integrations, UAT and QC.
  • Oncology clinical trial experience.
  • Ideally, C# custom functions and early-phase studies.


Why join?

The working environment genuinely sets these opportunities apart. The department has deliberately built a well-resourced team, promoting manageable workloads, collaboration and excellent work-life balance.


You'll have the freedom to contribute your expertise, help shape technical solutions and support meaningful oncology research within a business embracing the future of AI and clinical data.


We're looking for specialists in either discipline, not both.


If you're an experienced clinical programmer looking for stimulating work without the constant firefighting, we'd love to hear from you.

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