Overview In this role you will support the administration of clinical systems within Development Operations and collaborate with study teams to identify suitable sites for clinical studies. You will analyze data and provide inputs to select sites that meet study criteria, and assist with feasibility launches, including system setup and questionnaires. You will track responses, coordinate with stakeholders, and resolve feasibility issues while staying current on regulations and industry trends. This role offers the chance to influence site selection, forecasting, and study success in a fast-paced, cross-functional environment.

ResponsabilidadesEnsure CTMS data accuracy and integritySupport end users of clinical systems; process issue/enhancement requestsConduct research and data analysis to identify potential sites meeting study criteriaAssist feasibility launches,



including system setup and questionnaire outreachCoordinate with study teams and stakeholders to support feasibility activitiesTrack feasibility responses and report to internal stakeholdersTroubleshoot feasibility process issues (in-house and outsourced)Stay updated on regulations and industry trends related to site feasibilitySupport enrollment forecasting and discuss scenarios with stakeholders Requisitos principalesB.S. in a scientific or allied health field (or equivalent degree)3+ years of experience in clinical trial conduct/processes and/or 2+ years feasibility/recruitmentExperience with trial optimization vendors, tools, and methodsAbility to prioritize multiple projects within tight timelinesExperience working in multiple rare disease therapeutic areasExperience with data analysis and interpretationHighly proficient with Excelstrong communicationcross-functional collaborationprioritization and time managementCTMSExceldata analysis and interpretation

📌 Global Feasibility Specialist - Spain - IQVIA (Barcelona)
🏢 Jobrapido
📍 Barcelona