Senior Principal Statistical Programmer - Remote (Oncology)

BeiGene, Ltd.; Northern (KY); Hybrid; USD 144,000 - 189,000; Full time

Job summary

BeOne Medicines Ltd. seeks a (Senior) Principal Statistical Programmer to lead SAS programming across multiple oncology studies. You will manage deliverables, engage cross-functional partners, and ensure quality outputs for regulatory submissions and publications. Remote work from the US is supported.

The role requires 5+ years in SAS, CDISC expertise, and experience with FDA/EMEA submissions. Strong communication and project management skills are essential.

Qualifications

• Minimum 5+ years of clinical research programming using SAS.
• Expert-level knowledge and experience with CDISC methodologies (SDTM/ADaM).
• Experience leading or collaborating with centralized Statistical Programming teams.
• Experience in oncology trials.
• Experience with FDA/EMEA/CFDA submissions.
• Knowledge of drug development and project management fundamentals.
• Excellent verbal and written communication skills.

Responsibilities

• Technically lead and project manage multiple studies and study deliverables.
• Represent Programming at Study Management Team and Clinical Development meetings to address deliverables and timelines.
• Assess resourcing needs and staff projects accordingly.
• Review key study documents (SAPs, CRFs, DMPs, specifications, EDC data structures).
• Collaborate with Statisticians, Data Managers, Clinical Operations and Medical Monitors.
• Write, test, and validate SAS programs for analyses, tables, listings, graphs, and presentations.
• Develop and validate macros and utilities for reuse across studies.
• Interface with outsourcing partners and vendors.

Skills

SAS programming

CDISC (SDTM/ADaM)

Clinical trial experience

Regulatory submissions

Programming leadership

Education

Master's degree in Computer Science/Statistics/Life Sciences

Tools

SAS

Job description

BeOne Medicines Ltd. seeks a (Senior) Principal Statistical Programmer to lead SAS programming across multiple oncology studies. You will manage deliverables, engage cross-functional partners, and ensure quality outputs for regulatory submissions and publications. Remote work from the US is supported.

The role requires 5+ years in SAS, CDISC expertise, and experience with FDA/EMEA submissions. Strong communication and project management skills are essential.