Protocol Data Engineer for FDA POC

Jimmy Jazz

United States

Remote

USD 110,000 - 170,000

Full time

3 days ago
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Job summary

APV seeks a data engineering professional to operationalize structured protocol data models for FDA proof of concept. You will design scalable data structures, implement ETL/ELT pipelines, and ensure traceability and provenance across transformations and outputs in FDA-approved environments.

You will work with AI/prompt engineering, data standards, and interoperability SMEs to deliver robust, reviewer-friendly data solutions and dashboards tied to protocol evidence.

Qualifications

  • Extensive experience in database engineering, data architecture, and analytics.
  • Proven relational and dimensional modeling, ETL/ELT design, data quality.
  • Advanced SQL skills, PostgreSQL/PLpgSQL and Oracle PL/SQL experience.
  • Experience with AWS data services and cloud databases (Redshift, Aurora).
  • Experience integrating JSON/XML data and RESTful APIs; Python is a plus.

Responsibilities

  • Implement protocol data structures and physical schemas for protocol data.
  • Translate models into practical data-engineering components for POC.
  • Develop ETL/ELT pipelines with provenance, metadata, and reviewer feedback.
  • Support retrieval/semantic tooling and AI/prompt engineering collaboration.
  • Ensure QA, reconciliation, validation, and traceability for FDA review.

Skills

Database engineering
Data architecture
ETL/ELT design
Data warehousing
Data quality
Advanced SQL
PostgreSQL
Oracle PL/SQL
AWS data services
JSON/XML data integration
Python
CI/CD practices
FISMA/NIST controls familiarity

Education

BS degree in Computer Science, Mathematics, Data Science or relevant technical field

Tools

PostgreSQL
Oracle PL/SQL
SQL Server
AWS Redshift
S3
Glue
Lambda
DMS
Databricks
RESTful APIs

Job description

APV seeks a data engineering professional to operationalize structured protocol data models for FDA proof of concept. You will design scalable data structures, implement ETL/ELT pipelines, and ensure traceability and provenance across transformations and outputs in FDA-approved environments.

You will work with AI/prompt engineering, data standards, and interoperability SMEs to deliver robust, reviewer-friendly data solutions and dashboards tied to protocol evidence.

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