Teams at Kumquat Biosciences

Lead clinical operations for multiple global studies, overseeing COSLs, CRAs, vendors and CROs. Develop SOPs and metrics, manage budgets/timelines, ensure ICH-GCP and regulatory compliance, support rapid study start-up and database locks, drive inspection readiness, and mentor a high-performing operations team to deliver product development and regulatory milestones.

Provide legal support for Kumquat by drafting, reviewing, analyzing, and negotiating clinical, IT, R&D, quality, vendor, and confidentiality agreements; liaise with internal stakeholders, external parties, and CROs; ensure compliance with pharmaceutical regulations and data privacy; assist the General Counsel with ad hoc legal projects.