Teams at Rho (rhoworld.com)

Conduct onsite and remote clinical monitoring for MDD trials, performing site visits (PSV, SIV, IMV, COV), ensuring protocol and regulatory compliance, data audit readiness, site management, mentoring junior staff, contributing to protocol/study materials, and supporting business development and clinical operations initiatives. Up to 80% travel required.

Perform onsite and remote clinical monitoring (PSV, SIV, IMV, COV), ensure site adherence to protocol, ICH GCP, FDA and local regulations, maintain audit-ready documentation, mentor junior monitors, support site selection and RFPs, contribute to protocol/study materials, and conduct up to 8–10 site visit days monthly with heavy travel.

Maintain and enhance Excel-based pricing systems, analyze pricing requests, configure pricing logic, support proposal and contract pricing, collaborate with cross-functional teams, drive process improvements, deliver training and documentation, and ensure compliance and quality in pricing deliverables.