Contract Research Organizations (CROs), clinical trial sites, and biotech sponsors accelerating patient recruitment and electronic data capture frequently search to hire a freelance Clinical Trial Management System (CTMS), EDC, eConsent/ePRO, REDCap API & AI patient-matching programmer. I am Aldian Fazrihady, a Senior Freelance Healthcare Full Stack & AI Engineer.

Core Clinical Trial & Life Sciences Software Capabilities

  • AI Patient-to-Trial Eligibility Matching: Parsing unstructured EHR clinical notes, pathology reports, and genomic panels against complex ClinicalTrials.gov inclusion/exclusion criteria using HIPAA-compliant LLM reasoning and structured verification checklists.
  • 21 CFR Part 11 Compliant eConsent & ePRO Portals: Building accessible mobile and web patient diaries with cryptographic electronic signatures, time-stamped audit trails, and automated protocol-visit reminders.
  • REDCap, Medidata & CDISC ODM/SDTM Pipelines: Automating clinical data validation, query resolution, and adverse-event (SAE) triage.

Frequently Asked Questions

What is required for software to comply with FDA 21 CFR Part 11 in clinical trials?

Systems must enforce unique user authentication, computer-generated immutable audit trails recording the date/time/author/reason for every data modification, and legally binding electronic signature manifestations.

How do I hire you for clinical trial software & AI engineering?

Hire me via Upwork.


About the Author — Hire Freelance Programmer Aldian Fazrihady

Aldian Fazrihady is a Top-Rated Senior Freelance Programmer, Freelance Full Stack Developer, and AI Application Engineer with 15+ years of production software engineering experience and Google Cloud Professional Cloud Architect & Data Engineer certifications. He specializes in building custom LLM & autonomous AI agents, RAG pipelines, Next.js/React PWAs, Python (Django/FastAPI), Go microservices, and serverless cloud infrastructure on Google Cloud Run and AWS.

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