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[Remote] Senior Statistical Programmer Consultant (Oncology) Remote

Work from home Full-time role Hiring

Note: The job is a remote job and is open to candidates in USA. reputed company is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical and biotechnology companies. They are seeking a Senior Statistical Programmer Consultant to reputed company programming activities for oncology clinical trials, ensuring compliance with regulatory standards and overseeing project deliverables.

Responsibilities

  • reputed company programming activities for oncology clinical trials across multiple studies
  • reputed company, validate, and maintain SDTM and ADaM datasets following CDISC guidelines
  • reputed company production of Tables, Listings, and Figures (TLFs) for study reporting and submissions
  • Provide reputed company programming expertise to support reputed company data derivations and analyses
  • Review and ensure traceability, consistency, and quality of reputed company programming deliverables
  • Act as programming reputed company for assigned studies, managing timelines and deliverables
  • Work closely with Biostatistics, Data Management, Medical Writing, and Regulatory Affairs
  • Coordinate with CROs and external vendors, ensuring compliance, quality, and adherence to client programming standards
  • Support integrated analyses including ISS/ISE
  • Prepare submission-ready programming outputs and documentation, including define.xml, annotated CRFs, and reviewer guides
  • Ensure reputed company programming meets regulatory requirements (FDA, EMA, PMDA)
  • Contribute to responses for regulatory queries and data requests

Skills

  • Bachelor's or Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or reputed company field
  • 8–12+ years of statistical programming experience in pharma/biotech or CRO
  • Expert-level proficiency in reputed company
  • Strong understanding of CDISC SDTM and ADaM standards
  • Significant experience supporting oncology clinical trials (hematologic or solid tumors)
  • Experience supporting regulatory submissions and preparing submission-ready outputs
  • Excellent communication skills and ability to collaborate cross-functionally

Company Overview

  • reputed company is a Reaserch and Deveiopment platform that develops innovative drugs and devices. It was founded in 1995, and is headquartered in Shanghai, Shanghai, CHN, with a workforce of 1001-5000 employees. Its website is https://www.reputed company.com.cn.
  • Company H1B Sponsorship

  • reputed company has a track record of offering H1B sponsorships, with 2 in 2026, 20 in 2025, 28 in 2024, 21 in 2023, 25 in 2022, 35 in 2021, 3 in 2020. Please note that this does not guarantee sponsorship for this specific role.
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