Staff Oncology Data Product Manager

N-Power Medicine; Redwood City (CA); On-site; USD 168,000 - 215,000; Full time

Benefits offered by this job

Equity at hire

Discretionary annual bonus

401K plan

Job summary

N-Power Medicine is seeking a seasoned product leader to own the oncology data platform, aligning roadmaps with ProECA studies and regulatory expectations. You’ll define customers, success metrics, and drive adoption across biostatisticians, clinicians, and sponsors.

Collaborate with engineers, data architects, informaticists, and AI experts to deliver regulatory-grade data, provenance, CDISC specs, and robust data quality. Equity at hire and a competitive package await.

Qualifications

• 8+ years of product management experience owning a healthcare data product in a regulated environment.
• Deep background in oncology clinical data: AJCC staging, histology, biomarker and genomic testing, lines of therapy, RECIST-based response, progression, and survival endpoints.
• Working command of FDA guidance on externally controlled trials, use of EHR data in clinical investigations, 21 CFR Part 11, ICH GCP, CDISC (SDTM, ADaM), and HIPAA.
• Deep knowledge of EHR data structures and workflows (HL7, FHIR), clinical terminologies (ICD-10, SNOMED CT, LOINC, RxNorm, NCI Thesaurus), and data governance.
• Strong grounding in data platform architecture, data modeling, normalization, and transformation.
• Experience writing functional and technical specifications for data platforms.
• Strong analytical skills and data intuition: uses metrics to evaluate decisions and drive action.
• Exceptional written and verbal communication, with a track record of aligning oncologists, abstractors, biostatisticians, and engineers.
• Deep empathy for platform users, including quantitative scientists, epidemiologists, and study teams, and the ability to turn their needs into product requirements.

Responsibilities

• Own the vision, strategy, roadmap and requirements for the oncology data platform, aligned with N-Power's business goals and the needs of our ProECA studies.
• Manage the platform as a product: define its customers (biostatisticians, quantitative scientists, clinical operations, and pharma sponsors), set success metrics, and track adoption and value.
• Collaborate with a cross-functional team of engineers, data architects, informaticists, AI engineers, quantitative scientists, clinical abstractors, and medical oncologists.
• Build regulatory-grade evidence into the platform: source-to-dataset traceability across EHR and imaging, data provenance, audit trails, and fit-for-purpose data quality aligned with FDA guidance on external controls.
• Catalog and be able to point to end-user documentation for each data platform release: data dictionaries, vocabularies, CDISC-aligned specifications, data quality scorecards, licensing, and de-identification certifications.
• Produce external-facing collateral for pharma and health system partners: capability decks, platform architecture, marketecture, data flow diagrams, and the data roadmap.
• Prioritize relentlessly and manage trade-offs across various data use cases.
• Manage releases, build vs. buy decisions, and the impact of platform changes on active studies.
• Close process gaps in execution, rollout, and ongoing support through continuous stakeholder feedback.

Skills

Product management

Healthcare data

Oncology data

FDA guidance

EHR data (HL7/FHIR)

Data platform architecture

Specifications writing

Analytical skills

Communication

Empathy for users

Tools

Databricks

Snowflake

APIs

Job description

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.

Role Objectives and Responsibilities

• Own the vision, strategy, roadmap and requirements for the oncology data platform, aligned with N-Power's business goals and the needs of our ProECA studies.
• Manage the platform as a product: define its customers (biostatisticians, quantitative scientists, clinical operations, and pharma sponsors), set success metrics, and track adoption and value.
• Collaborate with a cross-functional team of engineers, data architects, informaticists, AI engineers, quantitative scientists, clinical abstractors, and medical oncologists.
• Build regulatory-grade evidence into the platform: source-to-dataset traceability across EHR and imaging, data provenance, audit trails, and fit-for-purpose data quality aligned with FDA guidance on external controls.
• Catalog and be able to point to end-user documentation for each data platform release: data dictionaries, vocabularies, CDISC-aligned specifications, data quality scorecards, licensing, and de-identification certifications.
• Produce external-facing collateral for pharma and health system partners: capability decks, platform architecture, marketecture, data flow diagrams, and the data roadmap.
• Prioritize relentlessly and manage trade-offs across various data use cases.
• Manage releases, build vs. buy decisions, and the impact of platform changes on active studies.
• Close process gaps in execution, rollout, and ongoing support through continuous stakeholder feedback.

Education, Experience, Behavioral Competencies, & Skills

• 8+ years of product management experience owning a healthcare data product in a regulated environment.
• Deep background in oncology clinical data: AJCC staging, histology, biomarker and genomic testing, lines of therapy, RECIST-based response, progression, and survival endpoints.
• Working command of FDA guidance on externally controlled trials, use of EHR data in clinical investigations, 21 CFR Part 11, ICH GCP, CDISC (SDTM, ADaM), and HIPAA.
• Deep knowledge of EHR data structures and workflows (HL7, FHIR), clinical terminologies (ICD-10, SNOMED CT, LOINC, RxNorm, NCI Thesaurus), and data governance.
• Strong grounding in data platform architecture, data modeling, normalization, and transformation.
• Experience writing functional and technical specifications for data platforms.
• Strong analytical skills and data intuition: uses metrics to evaluate decisions and drive action.
• Exceptional written and verbal communication, with a track record of aligning oncologists, abstractors, biostatisticians, and engineers.
• Deep empathy for platform users, including quantitative scientists, epidemiologists, and study teams, and the ability to turn their needs into product requirements.

Preferred

• Understanding of the oncology drug development lifecycle and how sponsors analyze data across clinical development, regulatory, and medical affairs.
• Experience with prospective clinical research operations: protocols, EDC, source data verification, monitoring, and inspection readiness.
• Experience with AI-assisted clinical data abstraction.
• Experience with data delivery and access platforms such as Databricks, Snowflake, and APIs.
• Agile delivery with tools such as JIRA.

Travel Requirements

Up to 25% travel

Pay Information

The expected salary range for this position is $167,777 - $215,304. 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.

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.

Applicants must be currently authorized to work in the U.S. on a full-time basis.

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 on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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.