Staff Oncology Data Product Manager

N-Power Medicine, Inc.

. Own the vision, strategy, roadmap, and requirements for the oncology data platform aligned with N-Power Medicine's business goals and ProECA studies .

Posted 11/5/2026full-timeRedwood City • California • United StatesLead💰 $167,777 - $215,304 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in product management for healthcare data platforms, with a strong focus on oncology clinical data, regulatory compliance, and data governance. Capable of translating user needs into actionable product requirements while ensuring data quality and adherence to industry standards.

Highest-signal resume keywords

Product Management ExperienceOncology Clinical Data ExpertiseFDA Guidance KnowledgeData Platform ArchitectureAgile Delivery with JIRA

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Oncology Clinical DataData ModelingData NormalizationFunctional Specifications WritingData GovernanceEHR Data StructuresData Quality ScorecardsBiomarker TestingGenomic TestingClinical Terminologies

Soft Skills

Exceptional CommunicationAnalytical SkillsStakeholder AlignmentProblem-SolvingCollaboration

Tools & Technologies

DatabricksSnowflakeAPIsJIRA

Industry Keywords

Clinical TrialsRegulated Environment21 CFR Part 11ICH GCPCDISCHIPAAAJCC StagingRECISTEHR DataClinical Research Operations

Tech Stack

Tools & technologies

Snowflake

About the role

Key responsibilities & impact

Own the vision, strategy, roadmap, and requirements for the oncology data platform aligned with N-Power Medicine's business goals and ProECA studies
Manage the platform as a product, defining customers, success metrics, adoption, and value
Collaborate with engineers, data architects, informaticists, AI engineers, quantitative scientists, clinical abstractors, and medical oncologists
Build regulatory-grade evidence, source-to-dataset traceability, data provenance, audit trails, and fit-for-purpose data quality into the platform
Catalog and provide end-user documentation for each data platform release, including data dictionaries, vocabularies, CDISC-aligned specifications, data quality scorecards, licensing, and de-identification certifications
Produce external-facing collateral for pharma and health system partners, including capability decks, platform architecture, marketecture, data flow diagrams, and the data roadmap
Prioritize and manage trade-offs across data use cases
Manage releases, build-versus-buy decisions, and the impact of platform changes on active studies
Close process gaps in execution, rollout, and ongoing support through continuous stakeholder feedback
Help advance N-Power Medicine's mission to transform clinical trials and bring better therapies to patients faster

Requirements

What you’ll need

8+ years of product management experience owning a healthcare data product in a regulated environment
Deep background in oncology clinical data, including 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
Exceptional written and verbal communication, with experience aligning oncologists, abstractors, biostatisticians, and engineers
Ability to turn platform users' needs into product requirements
Understanding of the oncology drug development lifecycle and sponsor data analysis across clinical development, regulatory, and medical affairs (preferred)
Experience with prospective clinical research operations, including protocols, EDC, source data verification, monitoring, and inspection readiness (preferred)
Experience with AI-assisted clinical data abstraction (preferred)
Experience with data delivery and access platforms such as Databricks, Snowflake, and APIs (preferred)
Agile delivery with tools such as JIRA (preferred)
Applicants must be currently authorized to work in the U.S. on a full-time basis
Company will not sponsor applicants for work visas
Up to 25% travel

Benefits

Comp & perks

Equity at hire
Discretionary annual bonus, potentially based on Company performance
Company benefits
401K plan
Balanced and flexible work environment
Competitive industry benefits
Other company perks