Job Details

Remote Biomedical Knowledge Systems Engineer (Part-Time, 20 hrs/week)

  2026-01-26     SIGMA     all cities,AK  
Description:

Remote Biomedical Knowledge Systems Engineer (Part-Time, 20 hrs/week)

Contract: 12 Months
Job ID: 36697593
Location: Fully Remote (U.S. candidates preferred)
Schedule: Part-Time - 20 hoursper week

About the Role

Sigma Systems is seeking an exceptionally specialized Biomedical Knowledge Systems Engineer to support and modernize a mission-critical scientific knowledge discovery platform used in biomedical and regulatory research.

This is a hands-on, senior-level engineering role requiring deep expertise across biomedical informatics, clinical trial data, FDA regulatory systems, GenAI-powered semantic search, and legacy system modernization. The ideal candidate will be comfortable owning complex systems end-to-end and working independently in a highly regulated, data-intensive environment.

Key Responsibilities

Legacy Biomedical Systems Ownership

  • Independently manage, maintain, refactor, and modernize a custom semantic scientific search platform
  • Troubleshoot and enhance legacy biomedical informatics applications with complex architectures
Biomedical Informatics Administration
  • Provide operational, administrative, and development support for:
    • Gene-Disease Association Knowledgebases
    • FDA Label Search systems
  • Maintain integrity of specialized biomedical data models and workflows
Advanced Data Migration & Modernization
  • Architect and execute complex document and vector database migrations
  • Perform large-scale migrations from MarkLogic to MongoDB
  • Ensure full metadata fidelity, auditability, and regulatory compliance
GenAI & Semantic Knowledge Discovery
  • Design and implement GenAI-powered applications for:
    • Semantic scientific search
    • Automated knowledge extraction
    • Cross-source biomedical data synthesis
  • Build and manage LLM and agentic frameworks, NLP pipelines, and knowledge graphs
  • Develop modern front-end interfaces using Vue.js (or equivalent)
Regulatory & Clinical Trial Analytics
  • Lead automated conversion of clinical trial results into FDA-compliant submission templates
  • Integrate data from FDA, AACT, and ClinicalTrials.gov
Cloud Architecture & Security
  • Support secure, compliant deployments in AWS
  • Work with EC2, Elastic Beanstalk, Secrets Manager
  • Advise on performance tuning, interoperability, and hybrid cloud best practices
Required Qualifications (Must-Have)
  • Bachelor's degree in Computer Science, Bioinformatics, Biomedical Informatics, or related field
  • 3+ years of dedicated experience in:
    • Biomedical software development
    • Specialized biomedical system administration
  • Mandatory hands-on expertise with BOTH:
    • MarkLogic
    • MongoDB
    • Including real-world migration experience between the two
  • Proven experience working with:
    • FDA data systems
    • AACT
    • ClinicalTrials.gov
  • Strong knowledge of FDA regulatory data standards
  • Direct experience with NLM biomedical data sources, including:
    • PubMed
    • PubMed Central (PMC)
    • Gene Expression Omnibus (GEO)
  • Production-level experience with:
    • NLP
    • GenAI / LLMs
    • Agentic AI frameworks
    • Semantic search and knowledge graph construction
  • Full-stack engineering expertise:
    • Frontend: Vue.js or similar
    • Backend APIs and microservices
    • Cloud-based scientific workflows
  • Experience deploying applications in regulated environments
Preferred Qualifications
  • Prior ownership or stewardship of custom-built biomedical information systems
  • Experience supporting or contributing to FDA regulatory platforms
  • Work involving scientific publication analytics or biomedical literature mining


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