Senior Manager, Scientific Programming

BeiGene, Ltd.; United States; Remote; USD 144,400 - 189,400; Full time

Job summary

BeiGene, Ltd. seeks a Senior Manager, Statistical Programming Project Lead who will be responsible for leading project development and overseeing programming deliverables across various development programs.

The candidate must have a Master's degree in a quantitative field and at least 5 years of experience in statistical programming. The role entails collaboration with clinical teams and contributing to regulatory submissions.

Salary range for this position is $144,400 to $189,400 annually.

Qualifications

• 5+ years of relevant experience in statistical programming.
• Experience with CDISC standards (SDTM, ADaM).
• Knowledge of clinical data structures and study designs.

Responsibilities

• Lead project development and oversee programming deliverables.
• Collaborate with Biostatisticians in strategic planning.
• Ensure programming meets industry standards.

Skills

Statistical Programming

Project Management

Regulatory Submission

Collaboration

SAS

Python

Education

Master's degree in a quantitative or scientific field

Tools

SAS (Base, Macro, SQL)

R

SQL

Job description

Senior Manager, Statistical Programming Project Lead

BeOne is recruiting a Senior Manager, Statistical Programming Project Lead to lead project development, oversee programming deliverables across multiple indication development programs.

Responsibilities

• Collaborate with lead project Biostatistician in strategic planning and provide guidance to the programming team.
• Create, implement, and maintain programming development plans for each project, accounting for timelines, resources, and quality deliverables.
• Ensure programming meets industry and internal standard practice.
• Represent the statistical programming team at Study Management Team and Clinical Development meetings to address deliverables and timelines.
• Contribute to development and implementation of programming resource algorithms.
• Collaborate with programming managers and project leads, lead resource planning and tracking.
• Interact and communicate with Statisticians, Data Managers, Clinical Operations, Medical Monitors, and Medical Writing to address programming related study deliverables.
• Contribute to strategies for programming related matters in submissions to regulatory agencies and publications.
• Understand and execute department, product, and study-level macros and utilities; write, test, and validate them.
• Serve as a technical resource for programming groups on complex tasks and standards.
• Assist in review of key study-related documents (e.g., SAP, CRF, data management plan, database specs, eDC structures, DMC plans).
• Oversee projects for creation of analysis datasets, production/validation of output, and review of annotated CRFs.
• Provide statistical programming support for FDA/EMEA/CDE regulatory submissions following CDISC standards.
• Contribute to departmental process and standards initiatives such as tools and CDISC standards.
• Collaborate and support selection and management of CROs, including strategic outsourcing providers.
• Oversee work in support of clinical trials, ad‑hoc analysis requests, data validation, etc.
• Lead development of TAUG (therapeutic area user guide) following CDISC industry standards.
• Other duties as assigned.

Qualifications

• Master's degree in a quantitative or scientific field (e.g., Computer Science, Statistics, Mathematics, Life Science) preferred.
• 5+ years of relevant experience in statistical programming.
• Experience with CDISC standards (SDTM, ADaM).
• Familiarity with regulatory submission deliverables (e.g., TFLs, ISS/ISE, eCTD).
• Knowledge of clinical data structures and study designs.
• Experience with ClinPharm/PK analyses.
• Familiarity with workflow automation and reproducibility.
• Ability to oversee multiple studies or programs.
• Vendor/CRO oversight experience.
• Cross‑functional collaboration with Statistics, Clinical, Data Management, Clinical Pharmacology, Medical Writing, and Regulatory.
• Proficiency in SAS (Base, Macro, SQL), R, Python, SQL.

Compensation

Salary range: $144,400.00 – $189,400.00 annually.

Equal Opportunity Statement

BeOne is a proud equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law.