Position Overview

Sr. Staff, Quantitative Sciences is a key leader in the Quantitative Sciences (QS) team and is responsible for ensuring that rigorous and fit‑for‑purpose statistical designs and analyses are performed to meet N‑Power Medicine’s vision and product claims. Working with a multidisciplinary team, this role will have the opportunity to fundamentally change the "how" of oncology clinical development. The Biostatistician works closely with other QS experts, Clinical Science, Product, Oncology Data Specialist (ODS)-certified professionals, and cross‑functional partners to conduct next‑generation external control arms (ECAs) that integrate retrospective and prospective real‑world data with single‑arm and randomized clinical trials. Through this collaboration, the leader also develops and ensures adherence to appropriate processes for data collection, ingestion, harmonization, standardization, quality control, management, analysis, and reporting.

Location: Hybrid on‑site in Redwood City, CA or Remote.

Role Objectives and Responsibilities

In collaboration with QS leaders, builds expert capabilities in prospective ECAs and hybrid controls combining retrospective and prospective real‑world data with single‑arm and randomized controlled trials.
Provides expertise for developing statistical methodologies that mitigate observed and unobserved selection, confounding, and measurement bias in external control and hybrid control studies utilizing retrospective and prospective observational data.
Guides and mentors internal teams on novel methodologies, best statistical practices, innovative clinical trial designs, statistical inference, and reporting statistical results.
Supports key strategic collaborations with life science partners.
Collaborates with the Data and Technology cross‑functional partners to define data requirements and data collections processes to enable next‑generation ECAs.
Leads or supports research study design and end‑to‑end delivery, in particular:
- Study scoping, including sample size calculations and identification of data needs.
- Design elements, and approach to bias mitigation in the design and analysis phases.
- Development of study protocols and statistical analysis plans.
- Leads or supports the execution of the analysis plan, including the development of adjacent algorithms and other scalable tools.
- Leads the communication of novel methodology developed in the course of the study. Co‑authors communications of study results in peer‑reviewed publications, presentations, and health authority reports.
Participates in internal, cross‑functional discussions on data and platform strategy, and workflow development.
Champions the development of tools, algorithms, and robust pipelines in support of study delivery, product offerings, data improvements, and efficiency, scalability, and reproducibility increases.

Education, Experience, Behavioral Competencies, & Skills

PhD in Statistics, or Biostatistics, with 6+ years of relevant experience in oncology clinical trials, biotech, and statistics.
6+ years experience in applying statistical methods to oncology patient data, including methods of advanced analytics and high dimensional data analysis.
3+ years as a Project Data Science Lead in a cross‑functional clinical development environment.
2+ years in oncology clinical trial statistics.
Expert knowledge of theoretical and applied epidemiology and statistics, including inferential methods for time‑to‑event analysis, survival analysis, and causal inference methods.
Expertise in design and analysis of externally controlled studies and hybrid controls including propensity score methods, endpoint measurement bias correction methods, and external patient borrowing Bayesian and frequentist methods.
Fundamental understanding of clinical‑ and efficacy endpoints used in oncology development.
Experience collaborating with clinical, biomarker, and imaging scientists, to apply statistical methods to oncology drug development.
Extensive experience with programming in R, SAS, and/or Python.
Strong communication and collaboration skills (including statistical consulting skills, and interpersonal skills).
Ability to work and collaborate in a fast paced, start‑up environment.
Entrepreneurial, credible and creative spirit capable of influencing stakeholders to advance the use of ECAs to inform Go no‑Go and regulatory decisions.
Excellent project management skills (including ability to manage scope and effectively delegate to other functions, staff, contractors and external vendors).
Excellent and autonomous drive for results (e.g., demonstrates interest and ability to learn new things, takes initiative, welcomes problems as challenges, proactively finds solutions to technical problems).
Generous, Curious and Humble.

Travel Requirements

Ability to travel may be required from time to time.

Pay Information

The expected salary range for this position is $186,000 and $259,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job‑related factors permitted by law. N‑Power Medicine offers equity at hire as well as a discretionary annual bonus which may be available based on company performance. This position is eligible for company benefits.

Equal Opportunity Employer

We are an Equal Opportunity Employer and value diversity at our company. We do not discriminate based on race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

Applicants must be currently authorized to work in the U.S. on a full‑time basis. The company will not sponsor applicants for work visas.

#J-18808-Ljbffr

Npowermedicine