Teams at ATS EA GH

Manage medical case processing and evaluate adverse events, review and triage ICSRs from clinical trials, author PSURs for regulatory submissions, detect safety signals, and perform risk-benefit evaluations to ensure regulatory compliance and patient safety.

Manage tech transfer and daily operations of mammalian or microbial bioreactor systems. Optimize cell culture, fermentation, and purification (chromatography/filtration). Ensure compliance with cGMP and FDA regulations, author SOPs, and investigate deviations using CAPA processes.

Design and scale data pipelines and algorithmic workflows to process NGS and multi-omic datasets, analyze population genetics to identify biomarkers, and collaborate with wet-lab scientists to validate findings.