Oncology Data Platform Product Lead

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

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.