Senior Software Engineer II

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Senior Software Engineer II in USA

Formation Bio
Full time
Email

USA
09/01/2026
Report

Boston, MA

Responsibilities

Own the design, delivery, and operation of production software used in live clinical trials from site startup through close-out.
Coordinate clinical, regulatory, data, infrastructure, QA, and validation dependencies to deliver software into active trials.
Build within a validated software development lifecycle and translate validation requirements into traceable, testable software.
Design and ship AI-native agents and pipelines that analyze clinical and operational data with provenance, audit trails, and human review.
Build integrations across EDC, CTMS, eTMF, CRO, laboratory, and safety-system data sources.
Own trial-specific domain logic and partner with Data Engineering on ingestion, orchestration, warehouse, quality, and governance capabilities.
Identify opportunities to shift trial activities earlier or run them in parallel through improved tooling.
Recognize GxP implications and engage QA and validation partners early in engineering decisions.
Set technical direction, review designs, mentor engineers, and improve organizational guardrails and automation.

Requirements

7+ years of experience building production software, including hands-on experience shipping software for use in a clinical trial.
Familiarity with clinical systems, clinical data flows, and the operational realities of active trial environments.
Experience with regulated or controlled software delivery, including GxP/GCP, computer system validation, requirements traceability, audit trails, electronic signatures, and change control.
Ability to translate regulatory requirements into compliant, maintainable, and well-engineered software.
Strong software-building skills with clean code, distributed-systems fundamentals, and cloud fundamentals using AWS, GCP, or Azure.
Daily experience with AI tools, LLMs, agentic workflows, and retrieval pipelines, with interest in responsible use in regulated clinical work.
Track record of technical ownership across multi-quarter efforts, cross-functional dependencies, and designs used by other engineers.
Ability to communicate effectively with clinical operations, QA, and other non-engineering stakeholders.
Comfort working with ambiguity and changing trial portfolios and roadmaps.

Benefits

Equity, comprehensive benefits, and generous perks are offered in addition to compensation.
Hybrid work model requiring 3 days per week in the office.
Hiring is focused primarily on the New York City and Boston metro areas, with consideration for candidates in the Research Triangle and San Francisco Bay Area; applicants must reside in or be willing to relocate to these locations.

Formation Bio

Formation Bio is an AI-native pharma company differentiated by radically more efficient drug development. The company has built proprietary technology platforms to optimize critical aspects of clinical drug development, enabling more efficient trial design, faster trial completion, and higher qua...

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