Overview In this role you will lead and oversee clinical trial monitoring as a senior CRA within Alira Health’s general Clinical team. You will work independently and with cross-functional partners to ensure protocol compliance, quality, and timely site visits across Spain and Europe. You will shape monitoring plans, mentor junior CRAs, and collaborate with sponsors to resolve site issues, driving project success and study timelines. This position offers exposure to international teams and a mission-driven, inclusive culture.

Compensaciones / Beneficiosremote workinternational teamcompetitive salary range 55k-70kfull-time contractlocation flexibility (Barcelona-Remote; Europe-Remote)professional development opportunities ResponsabilidadesProvide guidance and oversight to the CRA team to meet scope, SOPs, timelines, and budgetsReview monitoring visit reports and conduct co-monitoring and evaluation visits as neededCoordinate with cross-functional departments to resolve monitoring-related issuesAssist in development of monitoring plans and training materialsAssist in ethics documents setup and site contract negotiationProvide monthly billing information to financeManage study budget for monitoring stand-alone projects and act as sponsor referentPerform qualification, initiation, interim, and close-out visits both remotely and onsiteDocument monitoring visits with clear reports on problems, resolutions,



and enrollment statusEnsure data integrity through source document review and eTMF/TMF verificationConduct investigational product accountability and review regulatory bindersMaintain site communication to ensure GCP compliance and address sponsor requestsComply with ICH GCP, FDA regulations, and SOPs; participate in required meetingsFacilitate adverse event reporting and reconcile SAE with sources and CRFsCollaborate with CRAs, data management to resolve data discrepanciesIdentify site issues and develop problem-solving strategiesSupport CRA onboarding and mentoring; contribute to CTMS maintenanceManage conflicting priorities to deliver on commitmentsPerform additional duties as assigned Requisitos principalesBS/BA in life sciences or related discipline (US)3 years in pharma/biotech/CRO with 2 years clinical monitoring and 1 year management experience (US)EU: at least 2 years of clinical monitoring experience with capability to autonomously manage monitoring activitiesStrong knowledge of ICH GCP and regulatory requirementsExcellent communication and interpersonal skills; customer service orientationAbility to travel and manage stress; professional and trustworthyEnglish proficiency (US) or Local language proficiency (EU)Graduation in a scientific health field (EU)Adequate English (EU)quality-focusedhighly organized and multi-taskingproblem-solving and negotiationCTMS knowledgeeTMF/TMF documentation and verificationclinical trial databases and electronic data capture

📌 Senior Clinical Research Associate (Barcelona)
🏢 Jobrapido
📍 Barcelona