Jobs 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.

Perform onsite and remote clinical site monitoring (PSV, SIV, IMV, COV), ensure protocol and regulatory adherence, manage study documentation and audit readiness, mentor junior staff, support site selection and RFPs, and contribute to clinical operations and SOP development across multiple protocols with significant travel.

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.

Lead regional clinical trial operations and site management across multiple locations. Oversee site start-up, CRO/vendor contracting, IMP and supply logistics, regulatory/ethics submissions, monitoring and co-monitoring, recruitment and retention, budgeting and timelines, data clarification/cleaning, close-out activities, audits/inspections, and management of CRAs, CTCs and local study progress reporting.

Freelance regulatory consultant to proofread and adapt translated clinical trial labels to local requirements, review label printouts, approve documents, provide regulatory consulting for medicines (and preferably devices/IVDs), and interact with health authorities as needed. Ad hoc engagement (~1–2 hours/month) based in Moldova.

Process supplier invoices and employee expenses across multiple entities and currencies; ensure accurate coding, tax compliance, and approvals; manage vendor queries and vendor records; support payment runs, reconciliations, and month-end close; collaborate with international stakeholders.

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.

Support clinical data management activities including EDC study setup and validation, review and clean clinical data, program basic SAS listings, manage queries with oversight, review reconciliations and visualizations, and collaborate with lead data managers to ensure project execution.

Own and support accounting, month‑end/quarter/year‑end close, journal entries, reconciliations, intercompany activity, and statutory/tax reporting for assigned entities. Maintain audit‑ready documentation and internal controls, support audits, drive accounting process improvements, and use NetSuite/ERP and Excel to produce accurate financial reporting across multiple jurisdictions.