Teams at Castor

Lead complex, multi-component, multi-country clinical software studies from planning through delivery. Translate ambiguous scopes into operational project plans, coordinate internal teams and technical dependencies, manage risk, and guide customers toward effective solutions. Serve as a subject matter expert and consultative bridge between Castor and clients while ensuring clinical workflows, regulatory requirements, patient needs, and study objectives are addressed.

Own end-to-end clinical study builds, advising clients on CDMS, eCOA, patient-facing interfaces, and decentralized trial workflows. Lead consultation, configuration, scope management, and delivery timelines; identify technical issues and guide stakeholders through user acceptance testing. Apply clinical trial operations knowledge, software configuration skills, and compliance expertise across ICH-GCP, FDA 21 CFR Part 11, and GXP requirements.

Responsible for managing QA and release processes for core and client-specific software deployments in compliance with regulatory standards. Leads the QA team and ensures production readiness.