Search

SDTM Programmer

Redbock - an NES Fircroft company
locationSan Mateo, CA, USA
PublishedPublished: 6/14/2022
Technology
Full Time

Job Description

NO THIRD PARTIES


Position Summary

A clinical-stage biotech company based in the Bay Area is seeking a Senior Statistical Programmer to provide long-term contract support. The organization is focused on the development of oncology therapeutics, and with a growing pipeline, the programming team requires additional senior-level expertise.

This role will specifically focus on CDISC SDTM standards, requiring deep, hands-on experience in SDTM mapping and implementation for oncology clinical trials. The ideal candidate will be a subject matter expert in SDTM who can lead dataset development efforts, ensure regulatory compliance, and provide technical guidance to cross-functional teams.


Key Responsibilities

  • Lead the development, mapping, and implementation of CDISC SDTM datasets for oncology clinical studies.
  • Translate raw clinical data into compliant SDTM domains according to CDISC standards and sponsor requirements.
  • Develop and maintain SDTM specifications and mapping documentation.
  • Perform hands-on SAS programming to create, validate, and quality control SDTM datasets.
  • Ensure SDTM deliverables are submission-ready and compliant with regulatory standards.
  • Collaborate with Biostatistics, Data Management, and Clinical teams to resolve data and mapping issues.
  • Review CRFs, CRF annotations, and protocols to ensure accurate SDTM mapping.
  • Support regulatory submissions and respond to data-related queries as needed.


Top Requirements

  • 10–15+ years of statistical programming experience in clinical research, preferably with small to mid-sized sponsor companies
  • Extensive expertise in CDISC SDTM standards with strong hands-on SDTM mapping and implementation experience for oncology trials
  • Oncology experience required, with solid tumor experience strongly preferred (RECIST criteria)
  • Advanced SAS programming skills with a focus on SDTM dataset creation and validation.
  • Experience preparing SDTM datasets for regulatory submissions (e.g., FDA/EMA).
  • Ability to work independently and serve as an SDTM subject matter expert within the programming team.
  • Excellent communication skills and ability to collaborate effectively in a cross-functional environment.

Loading...
Loading...
Loading...
Loading...
Loading...
Loading...
Loading...
Loading...
Loading...
Loading...
Loading...
Loading...