Clinical Research Manager
Pubblicato il 04-10-2026 - Trial Form Support in Casagiove
OverviewAs 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 / Benefitscompetitive compensationlunch vouchershealth insurancepensioncar allowance where applicableResponsabilitàManage day-to-day clinical operations for assigned projects per protocol, contracts, and regulatory requirementsServe as primary sponsor contact for operational issues and study deliverablesLead and coach CRAs, ensuring completion of training requirementsOversee site quality and monitoring deliverables through direct supervisionDevelop and implement monitoring plans, site training plans, and verification initiativesCoordinate investigator meetings and country/site level reportingEnsure practical,
effective study processes from feasibility to closeoutProvide guidance to CRAs on site challenges and escalationsSupport recruitment and monitoring strategies to optimize study performanceConduct co-monitoring visits and review monitoring reports for timely issue resolutionReview CTMS data for accurate country/site/subject informationCollaborate on CRA onboarding, training, and handover with Project ManagersContribute to study communications and operational updatesOffer insights on resource utilization, revenue recognition, and forecastingParticipate in Investigator Meetings and present monitoring requirements when requiredPromote proactive issue resolution and a solution-oriented approachSupport business development initiatives, proposals, budget development, and bid defense activities as requiredRequisiti fondamentaliMinimum 5 years in clinical research with substantial on-site monitoring experience as a CRAAt least 1 year as an Unmasked CRA/CRM in an Ophthalmology studyExperience coordinating or overseeing clinical trial operations at study, country, or regional levelStrong understanding of clinical trial processes from startup through closeoutIn-depth knowledge of ICH-GCP, regulatory requirements, and clinical research standardsleadershipcommunicationproblem-solvingICH-GCPregulatory compliancemonitoring and quality oversight