Global Feasibility Specialist

Job SummaryThe Global Feasibility Specialist supports the administration of the clinical systems and tools utilized by Development Operations. Works in close collaboration with Development Operations teams, study start-up to provide key inputs, metrics, and outputs to support the selection of the most suitable sites for our clinical studies.
Summary of the Essential Functions of the Job Work with clinical study teams to ensure the accuracy of data in CTMSProvide support, under the direction of the Global Site Identification and Feasibility Manager or Senior Global Site Identification and Feasibility Specialist, to clinical systems end users, including receipt, evaluation and recommendation for all issue/enhancement requestsConduct research and data analysis to identify potential sites that meet the study criteria and objectivesAssist with feasibility launch to include system set-up, feasibility questionnaire creation and site-level feasibility questionnaire outreachEffectively communicating with study teams and relevant stakeholders as needed to coordinate and support additional feasibility activities as identified by the Global Site Identification and Feasibility Manager or Senior Global Site Identification and Feasibility SpecialistTracking and data entry of feasibility responses and reporting responses to the internal stakeholdersTroubleshoot any issues or discrepancies that arise in the feasibility process (in-house and/or outsourced studies)Stay up to date with current regulations and industry trends related to site feasibilitySupporting enrollment forecasting and discussing scenarios with internal or external stakeholders under the supervision of the Global Site Identification and Feasibility Manager or Senior Global Site Identification and Feasibility SpecialistMinimum RequirementsB.
S. in a scientific or allied health field (or equivalent degree) and 3+ years of experience demonstrating thorough understanding of clinical trial conduct and processes and/or 2+ years of feasibility/recruitmentExperience with trial optimization vendors, tools, and methodsAbility to prioritize multiple projects and tasks within tight timelinesExperience working in multiple rare disease therapeutic areasExperience with data analysis and interpretationHighly proficient with excelIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.
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SummaryLocation: Madrid, Spain; Barcelona, SpainType: Full time