15 ott - Belluno
Trial Form Support
Overview As Clinical Research Manager (CRM) in Ophthalmology, you lead clinical operations across multiple studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs, CRAs, sponsors, and sites. This role focuses on delivering trials on time, in scope, and to high quality, within a global CRO environment. Your work helps advance innovative ophthalmic therapies and improve patient outcomes. The position offers home-based work in Poland, Spain, or Italy and exposure to cross-functional, internationally distributed teams. Retribuzione / Benefits * competitive compensation * lunch vouchers * health insurance * pension * car allowance where applicable Responsabilità * Manage day-to-day clinical operations for assigned projects per protocol, contracts, and regulatory requirements * Serve as primary sponsor contact for operational issues and study deliverables * Lead and coach CRAs,
ensuring completion of training requirements * Oversee site quality and monitoring deliverables through direct supervision * Develop and implement monitoring plans, site training plans, and verification initiatives * Coordinate investigator meetings and country/site level reporting * Ensure practical, effective study processes from feasibility to closeout * Provide guidance to CRAs on site challenges and escalations * Support recruitment and monitoring strategies to optimize study performance * Conduct co-monitoring visits and review monitoring reports for timely issue resolution * Review CTMS data for accurate country/site/subject information * Collaborate on CRA onboarding, training, and handover with Project Managers * Contribute to study communications and operational updates * Offer insights on resource utilization, revenue recognition, and forecasting * Participate in Investigator Meetings and present monitoring requirements when required * Promote proactive issue resolution and a solution-oriented approach * Support business development i
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