Jobs at Rho (rhoworld.com)

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.

Manage clinical data lifecycle for trials: design CRFs, build and test EDC, create edit checks, lead data review/cleaning and reconciliation, support integrations and reporting, execute lock and closeout, ensure quality/compliance, coordinate cross-functional teams, and mentor junior staff.

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.

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.

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.

Lead and deliver complex global clinical research projects (respiratory focus), create project plans and risk strategies, manage resources and scope, mentor staff, oversee monitoring/CRA activities, collaborate with sponsors, and support BD activities.

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.

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.

Remote Poland-based data analyst supporting clinical trial reporting and Rave EDC builds. Develops and validates template notebooks, programs data listings, documents business rules, performs data quality audits, conducts descriptive and predictive analyses, and presents actionable insights to stakeholders. Identifies process improvements and implements statistical or mathematical methods as needed.

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.

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.