[Hiring] Clinical Data Manager @Viz.ai

Role Description

This is not a traditional eCRF-only Data Manager role. We are hiring a leader who can build and run research databases, operationalize EHR→EDC automation, and own data quality through data lock - while performing light-to-moderate statistical analysis as needed.

This position plays a critical role in driving Viz’s Evidence Generation strategy by managing the data life-cycle for clinical research and quality improvement studies. This role requires expertise in creating sophisticated data management systems, performing statistical analyses, automating data integrations, and ensuring robust data integrity practices.

Key Responsibilities

• Research Database Build & Full Data Management:
  • Configure/maintain EDC forms and eCRF specifications as needed to support ingestion and downstream analysis, focusing on scalability and standardization.
  • Own end-to-end Data Management for Evidence Generation studies: build, validate, and maintain research databases from ingest → cleaning → QC → data lock.
  • Develop and run data cleaning workflows (queries, reconciliation, audit trails), and ensure inspection-ready documentation.
• EHR → EDC Auto-Import & Data Model Strategy:
  • Design and operate data model strategy for automated ingestion of EHR-level RWE into the EDC.
  • Work hands-on with APIs/integration endpoints and unify disparate data models (site/EHR variability, mapping logic, versioning, schema evolution).
• EHR Systems Fluency / Site Data Reality:
  • Partner with site IT/informatics and the Product team to understand EHR constraints, extract structures, and change management.
  • Translate EHR data realities into feasible study data capture and monitoring plans.
• Collateral, SOPs, and Enablement:
  • Create and maintain DMPs, SAPs, SOPs, runbooks, and training materials that operationalize the above processes across care pathways.
• Statistical Analysis, as needed:
  • Perform statistical analyses on cleaned datasets (descriptive, comparative, time-to-event where appropriate) and support evidence packages and reporting.

You Will Thrive in This Role If:

• You possess advanced analytical capabilities, enjoy solving complex data problems, and have a deep interest in clinical research methodologies and outcomes.
• You are proficient in developing automated and scalable data solutions, and possess strong coding and database management skills (e.g., SQL, SAS, Python, R).
• You excel in strategic thinking and operational execution, adept at balancing immediate data management needs with long-term data infrastructure goals.
• You are highly organized, methodical, and meticulous about data integrity, compliance, and documentation standards.
• You enjoy collaborating with diverse stakeholders, effectively translating complex statistical concepts into actionable insights that drive clinical research forward.

Qualifications

• Required:
  • 5–7+ years in clinical research/RWE data management with hands-on database build + cleaning/QC ownership.
  • SQL + Python (or R) for data transformation, QC checks, and reproducible pipelines.
  • Experience with EHR or EHR-derived datasets and understanding of common structures/coding systems (ICD-10, CPT, LOINC, RxNorm preferred).
  • Practical familiarity with API-based ingestion and integrating multiple data sources/models.
  • Experience building/owning DMPs/SOPs/runbooks and maintaining audit-ready documentation.
  • Familiarity with integrating leading AI techniques into your work product.
• Preferred:
  • Experience with EDC platforms (Medidata Rave, REDCap, Castor, Veeva, etc.).
  • CDISC familiarity (SDTM/ADaM) or strong equivalent standardization experience.
  • Stats experience in real-world/implementation studies (propensity methods, time-to-event, mixed models) — not required to be a PhD biostatistician.

What success looks like:

• You are energized by building scalable, audit-ready Evidence Generation data systems; turning EHR-derived real-world data into clean, analysis-ready research datasets with minimal manual effort.
• You take end-to-end ownership of Research Databases (ingest → validation → cleaning → QC → data lock), and you continuously improve the EHR→Viz→EDC auto-import pipeline by designing resilient mappings, unifying disparate data models, and proactively troubleshooting data issues with sites and internal partners.
• You communicate clearly, document rigorously, and train teammates through lightweight SOPs, runbooks, and templates so the work scales across multiple care pathways.
• You manage competing priorities well and deliver on-time, high-quality outputs that support study milestones and sponsor expectations, while consistently practicing Viz core values.

After 90 days:

• There is visible improvement in data management execution - standardized database templates are in use, an agreed SDV/QA approach is documented, automated import performance is measured and improving, and stakeholders see faster turnaround on monitoring/cleaning and sponsor-ready reporting (with clear audit trails and reproducible outputs).

Why should you join us?

• If you are looking to make an impact, we are mission-driven and are making a difference in peoples’ lives every day.
• If you want to be a part of an amazing team, our people are the heart of everything we do.
• If you are a self-starter and naturally motivated, our work is driven by curiosity, innovation and team collaboration which allows us to leverage our skills immeasurably.
• We are a remote-first company across the U.S and EU, with a hybrid team in Tel Aviv.
• In the U.S, Viz offers competitive benefits, including medical, dental, vision, 401k, generous vacation, and other great benefits to full-time employees.