Teams at Iambic Therapeutics

Leads statistical programming for clinical trials from Phase I through regulatory submission. Designs, validates, and maintains SAS programs for SDTM, ADaM, and TLFs; ensures CDISC and FDA/EMA compliance; performs quality control; supports CSRs and submissions; mentors programmers; oversees vendors; and collaborates with biostatistics, clinical operations, data science, and machine learning teams.

Build agentic LLM systems that acquire, clean, validate, curate, and document large-scale biomedical datasets for multimodal model training. Develop reliable agent architectures, tooling, evaluation harnesses, quality-control workflows, and reproducible data pipelines. Collaborate with ML scientists, monitor distributed production pipelines, diagnose failures, and implement secure sandboxed execution with restricted access and audit logging.