- Location: Fully Remote (US Only) Must work PST hours
- Experience: 7+ years in full-stack software/product engineering, including technical leadership
Core Technical Stack (Non-Negotiable):
- Frontend: In-depth, hands-on expertise in Angular 17+, TypeScript, RxJS/signals, typed Reactive Forms, state management, and real-time/collaborative UI patterns.
- Backend: Strong production experience in Python with FastAPI (or comparable), Pydantic contracts, SQLAlchemy/ORM, and async job handling.
- Cloud & Data: PostgreSQL/SQL, AWS, Kubernetes/EKS, CI/CD.
Domain Requirements (Highly Critical): Candidates must have direct software engineering experience in Life Sciences, Biotech, Pharma, or Clinical Trial Technology (e.g., EDC, eCOA, CTMS, Protocol Digitization).
- Project Context: The product is a digital authoring and collaborative platform used by clinical scientists to build, version, and structure Clinical Study Protocols in a regulated environment.
- Key Concepts/Keywords: Protocol Digitization, Study Builder/Designer, CDISC, USDM, GxP, CSV (Computer System Validation), 21 CFR Part 11, ALCOA+, Electronic Signatures, Immutable Audit Trails.
- Target Backgrounds: Profiles from Clinical SaaS vendors (e.g., Veeva, Medidata, IQVIA), Pharma/Biotech digital labs, CROs, or Life Sciences tech consultancies.
Sign in
To continue your applicationor continue with email
By continuing you agree to our Terms & Privacy Policy.
Similar jobs
