Senior Statistical Analyst # 4622

GRAIL

1d • Remote

About The Position

Our mission is to detect cancer early, when it can be cured. We are working to change the trajectory of cancer mortality and bring stakeholders together to adopt innovative, safe, and effective technologies that can transform cancer care.

We are a healthcare company, pioneering new technologies to advance early cancer detection. We have built a multi-disciplinary organization of scientists, engineers, and physicians and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicine’s greatest challenges.

GRAIL is headquartered in the bay area of California, with locations in Washington, D.C., North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies.

For more information, please visit grail.com

This role is part of the Clinical Biostatistics group within the Clinical Development organization at GRAIL. The Senior Statistical Analyst contributes to the analysis of clinical study data through their statistical programming expertise. This individual will develop programs for and maintain complete and auditable documentation of the analysis of GRAIL’s clinical studies.

This role is approved to work remotely in California. While the primary workplace is form home, it may be required to travel occasionally to a GRAIL office or other locations to perform work or attend team-related events.

Requirements

• Minimum 4 years statistical programming experience in academia or industry is required.
• Experience in a similar industry as GRAIL is preferred.
• B.S. in Statistics or related fields.
• Proficient in R or Python or SAS
• Ability to work independently on multiple concurrent projects in a fast-paced environment
• Strong team player with demonstrated track record of success in cross-functional team environment

Nice To Haves

• M.S in Statistics or related fields preferred.
• Proficiency in R is strongly preferred.
• Knowledge of applicable regulatory rules and guidelines, e.g., ICH, GCP, HIPAA, is preferred.

Responsibilities

• Provide statistical programming support to pre-defined and exploratory analysis, formal reports, publications, presentations, and new statistical methodologies
• Manage the timeline and deliverables of the analysis dataset and Tables, Figures and Listings (TFL) development
• Work closely with biostatisticians to review the statistical analysis plan (SAP), and create data and analysis program specifications based on the SAP and TFL shells
• Maintain complete and auditable programming documentation for analysis of clinical studies
• Contribute to the development, documentation and maintenance of a reusable programming code library
• Serve as a member of clinical study teams
• Stay abreast of industry developments in the Statistical Programming field and apply to appropriate systems and processes

Benefits

• flexible time-off or vacation
• a 401(k) retirement plan with employer match
• medical, dental, and vision coverage
• carefully selected mindfulness programs

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level