🕒 2 days ago
Leads product safety for complex clinical studies, overseeing safety governance, case processing, reporting, sponsor communications, study plans, timelines, and quality while guiding junior team members.
Rhoworld jobs
A global CRO providing clinical trial strategy and services from first-in-human studies through approval.
🏢 Healthcare🏥 Clinical Research
8 open roles at Rhoworld
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🕒 3 days ago
Leads clinical study start-up from feasibility through site activation, coordinating regulatory and ethics submissions, essential documents, budgets, contracts, timelines, and cross-functional teams to support timely delivery.
🕒 3 days ago
Support clinical trial monitoring by managing essential documents, study tracking systems, and data reviews while coordinating with CRAs and study teams, with the opportunity to grow into a traveling CRA role.
🕒 5 days ago
Support clinical trial monitoring by managing essential documents, study tracking systems, and data reviews while coordinating with CRAs and study teams and building experience toward a traveling CRA role.
🕒 5 days ago
Coordinate clinical study start-up from feasibility through site activation, supporting regulatory and ethics submissions, essential documents, informed consent forms, site budgets, contracts, and timely handoffs.
🕒 20 days ago
Leads clinical operations for assigned research projects, overseeing site and CRA performance, study planning, risk management, compliance, and team training to drive successful trial delivery.
📍 🇺🇸 United States - Remote💰 $130k - $150k / year💼 Full-Time🎸 Senior🏥 Clinical Operations Specialist
🕒 26 days ago
Provide medical and scientific oversight across clinical trial projects, advising teams and sponsors on trial safety, design, conduct, and regulatory considerations across multiple therapeutic areas.
📅 Apr 17, 2025
Review and adapt translated clinical trial labels to local regulatory requirements, advise on clinical trial regulations, and liaise with health authorities when needed.
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