Skip to Main Content

Job Title


Global Site Identification and Feasibility Specialist (Canada)


Company : ICON Strategic Solutions


Location : windsor, Ontario


Created : 2025-05-05


Job Type : Full Time


Job Description

As a Global Site Identification and Feasibility Specialist you will be joining the worlds largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:Work with clinical study teams to ensure the accuracy of data in CTMS.Provide 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 requests.Conduct 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 outreach.Effectively 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 stakeholders.Troubleshoot 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 SpecialistYou are:B.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 methodsAnalytical thinker with great attention to detail;Good knowledge of concepts of clinical research and drug developmentExperience collaborating with internal and external stakeholdersAbility to prioritize multiple projects and tasks within tight timelines;Excellent written and verbal communication skills.Demonstrated administrative and project management abilities in an academic, CRO or sponsor environment