Expertise: Ensures application of appropriate, basic statistical methods and generation of accurate and reproducible results. Produces clear, concise, well-organized, and error-free analysis programs and statistical reporting content. Is able to handle all levels of analysis complexity and can work independently;

Quality and Compliance: Complies with organization and company standard operating procedures in timely fashion, such as training and project time accounting. Understands and aligns with relevant regulatory guidance. Ensures that documents, specifications, programs, and macros are consistent and comply with project and company standards. Follows best practices for Data Integrity. Documents projects in sufficient detail for reproducibility, including entry in project tracking systems and placement into shared repositories;

Drug Development: Assists in providing experimental design, modeling, analysis planning, analysis execution, interpretation and statistical communications support. Is accountable for the execution of individual project responsibilities, including: meetings with necessary project team members, reporting activities, exploratory analyses/graphics, and additional analyses to support publications for individual clinical trials/studies/projects. Is able to support program-wide strategic analyses, including Health Authority responses;

Collaboration: Establishes and maintains effective and efficient interfaces and relationships with internal and external customers, with support of Statistics & Decision Sciences (SDS) management;

Programming: Expert in SAS or R;

Process: Basic knowledge of data architecture and formats, such as Data Standards

Education: Master degree or above

Experience: at least 1 year’s statistician experience;

Knowledge of SAS or R programming; (See levels above under Programming)

Good written, oral, and interpersonal communication skills