Jobs at Rho (rhoworld.com)

Manages clinical study sites from feasibility and selection through initiation, routine monitoring, close-out, and file maintenance. Ensures data quality, regulatory and SOP compliance, timely study completion, and budget adherence. Responsibilities include Ethics Committee and Regulatory Authority submissions, site contract support, and country feasibility. Requires clinical research experience, strong communication in English and local languages, attention to quality, adaptability, a driver’s license, and travel availability.

Conduct site feasibility, selection, initiation, routine monitoring, close-out, and study file maintenance for assigned clinical studies. Ensure data quality, regulatory and SOP compliance, and timely, budget-conscious study completion. Prepare Ethics Committee and Regulatory Authority submissions, assist with site contract management, and communicate effectively with sponsors and sites. The role requires clinical research experience, English and local-language fluency, a driver license, and travel availability.

Manages clinical study sites across feasibility, selection, initiation, routine monitoring, close-out, and file maintenance. Ensures data quality, ICH-GCP and SOP compliance, regulatory adherence, and timely, budget-conscious study completion. Responsibilities include country and site feasibility, Ethics Committee and Regulatory Authority submissions, site contract assistance, and ongoing communication with sponsors and sites. Requires at least two years of on-site monitoring experience, relevant life sciences education, English and local-language fluency, a driver’s license, and travel availability.

Manages clinical trial data across study design, EDC build, CRF development, data review, cleaning, reconciliation, reporting, database lock, and closeout. Collaborates with biostatistics, programming, clinical operations, sponsors, and vendors. Ensures compliance with standards, SOPs, RBQM, and QbD principles while identifying risks and improving processes. Coordinates multiple projects, tracks KPIs, supports audits, and mentors team members.

Conduct site feasibility, initiation, routine monitoring, and close-out visits for assigned clinical studies. Manage site administration, prepare regulatory and ethics submissions, support site contracts, and ensure compliance with sponsor procedures, legal requirements, and ICH-GCP. The role requires at least two years of on-site monitoring experience, fluency in English and local languages, strong communication skills, a driver’s license, and travel availability. Major Depressive Disorder experience is preferred.

Conduct and coordinate clinical trial monitoring across multiple protocols, including site visits, site management, documentation, data quality, audit readiness, corrective actions, and study closure. Support protocol development, site selection, investigator meetings, training, and business development activities while mentoring junior clinical team members. The remote role requires residence within one hour of a U.S. metropolitan airport and travel up to 80% for 8–10 site-visit days monthly.

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.

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.

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.