Teams at Rho (rhoworld.com)

Lead and manage study start-up activities through site activation, regulatory and ethics submissions (including CTIS Part 2), feasibility, SIV/activation planning, site contracts and budgets, and oversight of SSU associates while collaborating with project and clinical leads and sponsors.

Provide remote trial documentation and TMF/CPF management support, upload site and country documents to Veeva Vault, prepare ISFs and submission packages, assist CRAs and Trial Manager with data entry, meeting minutes, tracking, stakeholder communication, and support audits/inspections.

Perform onsite and remote clinical site monitoring (PSV, SIV, IMV, COV), ensure protocol and regulatory compliance, maintain audit-ready data, mentor junior staff, contribute to protocol development and RFPs, and manage relationships with clinical sites while supporting clinical operations initiatives.