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N-Power MedicineNM

Senior Clinical Data Scientist, Data Products & Insights

N-Power Medicine is a clinical research and drug development platform company focused on accelerating oncology drug development by integrating clinical research into routine patient care.

N-Power Medicine

Employee count: 51-200

Salary: 130k-167k USD

United States only

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

N-Power Medicine is hiring a Senior Clinical Data Scientist to lead the development of scalable data products, analytical endpoints, and research studies leveraging real-world data (RWD), prospective external control arms (ECAs), and other advanced healthcare data sources.
This role sits at the intersection of data science developer and product owner: you will design, build, and maintain reproducible R-based tools and analytics frameworks while shaping product requirements and ensuring adoption by internal and external stakeholders. Success means delivering robust, validated analytics capabilities that accelerate clinical research, democratize access to data and insights, and empower teams across the organization to make evidence-based decisions.
This position is remote within the United States.

Role Objectives and Responsibilities

  • Develop analytics endpoints and frameworks in R for prospective ECA and retrospective RWD studies, ensuring reproducibility, transparency, and scalability across multiple indications.
  • Design and own reusable data science tools/products that enable broader teams—clinical, product, biostatistics, and external collaborators—to access data, derive insights, and run analyses without deep programming expertise.
  • Create standardized, validated endpoints that can be used repeatedly across studies, accelerating timelines and improving comparability of results.
  • Collaborate with cross-functional teams to define requirements, prioritize features, and deliver solutions that are intuitive, scientifically rigorous, and research-ready.
  • Act as both builder and product leader: scope, prototype, and productionize solutions while ensuring they align with broader business strategy and are adopted by stakeholders.
  • Champion democratization of data and insights by building tools, documentation, and workflows that expand access and usability across the organization and network.
  • Mentor and guide teammates, contributing to a culture of technical excellence, transparency, and knowledge-sharing.
  • Engage externally with collaborators, sponsors, and scientific partners to demonstrate the rigor and impact of our analytics solutions.
  • Perform other duties as assigned to support team and company goals.
Education, Experience, Behavioral Competencies, & Skills
  • 5+ years of progressive experience in data science and healthcare research.
  • Bachelor’s degree or equivalent experience.
  • Deep expertise in R programming (package development, reproducible pipelines, RMarkdown/Quarto, Shiny, tidyverse/dplyr).
  • Experience with clinical research data (RWD, EHR/EMR, claims, registries, clinical trial data).
  • Proven track record of building scalable, validated analytical tools that empower non-technical users to generate insights.
  • Demonstrated ability to translate technical capabilities into accessible, productized solutions used across teams.
  • Excellent communication skills and ability to engage both technical and non-technical stakeholders.
  • Bias for action and problem solving - we are looking for builders to join the team and help us build toward a big vision.
  • Generous, Curious & Humble.

Preferred:

  • Experience with external control arms (ECAs) and prospective RWD studies, preferably with experience in oncology.
  • Strong understanding of causal inference, survival analysis, and endpoint development in regulatory-relevant contexts.
  • Familiarity in working with Life Sciences teams at large pharma organizations.
  • Knowledge of data engineering practices (version control, CI/CD, workflow orchestration).
  • Leadership experience mentoring junior data scientists.

Travel Requirements

Ability to travel may be required from time to time.

Pay Information

The expected hourly range for this position is $130,000 and $167,000. 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 at 30+ hours/week.

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.”
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.
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.
Notice on fraudulent job offers: Only positions posted on https://npowercareers.multiscreensite.com/ site are legitimate. Please be mindful of recruitment fraud and job scams.

About the job

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Posted on

Job type

Full Time

Experience level

Senior

Salary

Salary: 130k-167k USD

Location requirements

Hiring timezones

United States +/- 0 hours

About N-Power Medicine

Learn more about N-Power Medicine and their company culture.

View company profile

At the heart of N-Power Medicine is a culture driven by the core values of Empowering Community through generosity, curiosity, and humility. These principles form the bedrock of our company culture, guiding our mission to revolutionize the clinical trial process and accelerate the development of life-saving oncology drugs. We believe in leading by prioritizing the success of others and fostering an environment where sharing opportunities, knowledge, and support is paramount. Our team is a diverse, multi-disciplinary group with expertise spanning healthcare, engineering, technology, and regulatory fields. We are committed to building an exceptional workplace where every member can thrive, grow, and achieve their full potential. This commitment extends to the broader community, as we aim to make clinical research an integral part of every oncologist's practice and every cancer patient's care.

Our vision is to radically accelerate drug development timelines by creating a new model where participation in advancing new therapies is readily accessible. We address critical challenges faced by oncology sites by seamlessly integrating technology and trained personnel into routine care. This 'human in the loop' approach, which combines virtual and on-site staff with AI-enabled workflow automation, supports oncologists in generating research-ready data for all patients and preparing standardized clinical documentation. By unlocking the full potential of every patient's data, we strive to bring innovative therapies to patients sooner. We are dedicated to fostering critically needed innovation within the cancer care ecosystem, ultimately benefiting patients in urgent need of new treatments. Our commitment to diversity, equity, and inclusion is unwavering, as we believe that a variety of perspectives is essential to achieving our ambitious goals.

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