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Truveta

Analyzes health records for medical research

Principal Privacy Biostatistician - Risk Analytics

Privacy & Data ProtectionConfirmed live in the last 24 hours
Full-timeSeattle, WA, USAHybrid

About the Job

Requirements

  • A PhD in biostatistics, statistics, epidemiology, or a related quantitative field, or a master's degree with equivalent depth of experience and demonstrated technical leadership is required.
  • At least 10 years of experience in statistical methods applied to patient health information, including extensive hands-on experience in statistical disclosure control and de-identification, is required.
  • Prior formal Expert Determination signing experience under HIPAA, internally or as an external consultant or expert witness, with a documented case history across multiple data modalities, is required.
  • A proven track record of defining and implementing de-identification methodology at an organizational or platform level, rather than only on individual datasets, is required.
  • Deep experience with multiple non-structured data modalities, such as imaging and/or clinical notes, in addition to structured EHR or claims data, including risk across linked modalities, is required.
  • Expert-level ability to reason across the HIPAA Privacy Rule and Security Rule boundary when estimating risk is required.
  • Exceptional written and verbal communication skills are required, including producing documentation that stands alone under audit and explaining complex risk concepts to executives, partners, and regulators.
  • Experience analyzing Real World Data in a research setting is required.
  • Demonstrated success mentoring senior technical staff and developing others toward independent signing authority is required.

Responsibilities

  • Set the vision and own the end-to-end statistical disclosure control framework for Truveta's data platform, defining the methodological standards, risk thresholds, and documentation requirements used by the entire Risk Analytics team.
  • Serve as a signing Expert Determiner for the most complex, novel, and high-visibility data products, applying generally accepted statistical and scientific principles to determine that re-identification risk is very small, and documenting the reasoning to a standard that stands on its own under audit, regulatory review, or legal challenge.
  • Act as the final technical reviewer and co-signer for Expert Determinations prepared by Senior and staff Privacy Biostatisticians, and establish and run the peer-review and case-defense process that governs the team's signing authority.
  • Lead the development of risk methodology for new and emerging data modalities, including genomic data, linked multi-modality data, and AI/ML-derived data products, partnering with clinical informatics, Legal, and Product to define Truveta's approach before these products go to market.
  • Own and continuously evolve profile-level risk-justification methodology, including dynamic k-anonymity thresholds, quasi-identifier importance ranking, suppression hierarchies, drift-triggered re-determination thresholds, and process-level Expert Determinations, ensuring it scales with platform growth.
  • Integrate Truveta's HIPAA Security Rule posture into Privacy Rule risk determinations, and partner with security and engineering leadership to influence infrastructure, architecture, and regulatory change strategy.
  • Partner with Legal and Contracts to define the organization's standards for supplementary recipient-side controls on higher-residual-risk modalities, while reinforcing that these controls do not substitute for the statistical very-small-risk determination.
  • Represent Truveta as the privacy statistics subject-matter expert with health system members, customers, auditors, and regulators, and contribute to external publications, conference presentations, and industry standards.
  • Mentor and develop Senior and staff Privacy Biostatisticians, building a clear, documented pathway toward independent signing authority and growing the team's overall bench strength.
  • Influence product and data strategy by identifying opportunities to improve data utility and usability while managing residual risk and mitigating controls across the platform.

Desired Qualifications

  • Experience defending Expert Determinations in regulatory, audit, litigation, or expert-witness settings.
  • Experience designing and governing process Expert Determinations at scale.
  • Advanced hands-on experience with SDC tools such as sdcMicro and dynamic or continuously revalidated risk methodologies.
  • Working familiarity with clinical informatics standards, including HL7, FHIR, and DICOM PS3.15 Annex E.
  • Hands-on experience with genomic data privacy, including VCF-level re-identification risk and familial risk.
  • A record of peer-reviewed publications, conference presentations, or contributions to industry standards in privacy, disclosure control, or health data.
  • Experience building or leading a privacy statistics or risk analytics function.

About the Company

Truveta

Analyzes health records for medical research

Truveta sells health data and research software to life sciences companies, public health teams and healthcare organizations studying diseases, drugs and medical devices. Its platform organizes de-identified patient records into longitudinal datasets and normalizes clinical information into standard medical terminology for analysis. Researchers build cohorts and examine treatment patterns in a cloud workspace, while Truveta Intelligence translates plain-language questions into structured analyses. The company sells data subscriptions and supplies evidence services spanning study design, custom analytics and research delivery. Truveta was founded in September 2020.

Company size
201-500
Company stage
Late Stage VC
Total funding
$515M
Headquarters
Bellevue, WA
Founded
2020

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