Sr. Staff Data Scientist, Biostatistics at N-power Medicine Redwood City, CA

Sr. Staff Data Scientist, Biostatistics job at N-power Medicine. Redwood City, CA.

About N-Power Medicine

N-Power Medicine aims to establish a new paradigm in drug development by reinventing the ‘how’ and transforming clinical trials through better integration with clinical practice, ensuring broader participation by physicians and patients. We are building an exceptional multi-disciplinary team with diverse expertise spanning healthcare, engineering, technology and regulatory, and with people who share our core value of Empowering Community through generosity, curiosity and humility. We are working with urgency to bring better therapies to patients faster.

Position Overview

The Sr Staff Data Scientist, Biostatistics 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 NPM’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. This responsibility includes working in close collaboration with other QS experts, Clinical Science, Product, Oncology Data Specialist (ODS)-certified professionals and other 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 Biostatistics leader also works cross-functionally to develop and ensure adherence to appropriate processes for data collection / ingestion, harmonization, standardization, quality control, management, analysis and reporting.

We are open to 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.
• Collaborates with Clinical Science and Commercial teams to provide statistical leadership for innovative clinical development projects, including providing strategic input into clinical study plans and protocols, regulatory strategy, target product profiles (TPPs), and integrated evidence plans.
• 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

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 (NPM) 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.

More About Us

We are a mission-driven, well-funded, rapidly growing company, eager to attract passionate professionals offering a highly attractive compensation package with a balanced and flexible work environment, competitive industry benefits as well as a 401K plan and other great company “perks.”

Equal Opportunity

We are an Equal Opportunity Employer and value diversity at our company. We do not discriminate based upon 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.

Covid-19 Policy

The Company is committed to providing and maintaining a safe workplace, and to safeguard the health and well-being of our employees, families, visitors, and the community. While vaccination remains one of the most important tools in advancing the health and safety of employees and promoting the efficiency of workplaces, we are now in a different phase of our response when these measures are no longer necessary. We currently do not have mandatory COVID-19 vaccination requirements for our employees and contractors, as the COVID-19 public health emergency has ended. However, there are certain N-Power Medicine employees and contractors who, based on their role, will be required to continue to follow our 2021 COVID-19 vaccination and other requirements as mandated by N-Power Medicine’s partners they serve. We reserve the right to modify or amend our corporate policy at any time.

Work Authorization

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.

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