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(Part-time, contractor) CTMS Platform Builder & Technical Product Manager

Onsite or remote • San Francisco+1💼 Part-time🗓 2026-06-25

Core

Full-stack developer and technical product manager owning the CTMS platform, building participant-facing workflows, operational tools, and compliance systems for clinical trials.

Role type

Senior IC full-stack developer (technical product manager)

Builds

Production CTMS infrastructure, participant portals, study coordination tools, and compliance workflows

Domain

Healthcare / Clinical Trials / Healthtech

Deliverable

production ML models | product features | infrastructure

Required skills

Full-stack development (backend-heavy, API design, database, server-rendered frontends), HIPAA compliance and PHI handling, Clinical trial systems experience (CTMS/EDC, 21 CFR Part 11, GxP), AI-assisted development (Claude Code, Cursor, Windsurf, Copilot)

Responsibilities

Build and maintain participant-facing workflows and internal operational tools, Design secure systems for kit activation and clinical data handling, Develop coordinator workflows and reporting dashboards, Improve communication systems and participant engagement infrastructure, Support compliance, auditability, and operational reliability, Contribute to CTMS architecture evolution, Collaborate on infrastructure and scalability decisions, Explore intelligent automation and AI-assisted workflows

Seniority

Senior, hands-on IC

Rewrite
## About the Role We're looking for a full-stack developer who doubles as a technical product manager to take ownership of our CTMS platform. You'll work with AI-assisted development tools (Claude Code, Cursor, or similar) alongside strong engineering fundamentals to ship features fast, manage the product roadmap, and handle deployment. This is not a "write specs and hand off" PM role. You will build, ship, and deploy — with AI tools accelerating code generation while you provide the architecture, security judgment, and quality control. The system has two main portals: - Study Admin Portal — for Taxa staff (coordinators, PIs, operations) - Participant Portal — mobile-first interface for study participants ## What You'll Own You will help scale and productionize Taxa's clinical operations platform and next-generation CTMS infrastructure across participant logistics, study coordination, compliance workflows, and automation systems. Key areas of ownership may include: - Building and maintaining participant-facing workflows and internal operational tools - Designing secure systems for kit activation, participant tracking, and clinical data handling - Developing coordinator workflows, reporting tools, and operational dashboards - Improving communication systems, notifications, and participant engagement infrastructure - Supporting compliance, auditability, and operational reliability requirements - Contributing to the evolution of Taxa's CTMS architecture and operational data systems - Collaborating on infrastructure, security, and platform scalability decisions as the system evolves - Exploring intelligent automation and AI-assisted operational workflows This role requires strong product-minded engineering judgment, comfort operating in ambiguity, and the ability to make pragmatic architectural decisions in a fast-moving environment. ## Required Skills - Full-stack development — backend-heavy (API design, database, integrations), comfortable with server-rendered frontends - HIPAA / healthcare data handling — experience with PHI storage, encryption requirements, audit trails, and BAA chains. Must be able to articulate your approach to HIPAA compliance in the proposal - Clinical trial or healthtech experience — prior work with participant management, DCT workflows, CTMS/EDC systems, or regulated software (21 CFR Part 11, GxP, or equivalent) - AI-assisted development proficiency — experience with Claude Code, Cursor, Windsurf, Copilot, or similar AI coding tools. You
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