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Conduct global site identification and feasibility activities to support clinical trial start-up Analyze data sources and study requirements to identify and prioritize suitable investigator sites Review clinical trial protocols and translate study requirements into clear site profiles Perform site vetting and qualification assessments based on feasibility criteria and site capabilities ...
About the Role
About the Role
We are seeking an experienced Global Site Identification Specialist to support clinical trials through targeted site identification and feasibility activities. This role plays a critical part in ensuring the selection of high-performing investigative sites aligned with study requirements.
Working closely with global study teams, you will combine clinical expertise, data analysis, and operational insight to identify, evaluate, and engage potential sites across Europe.
Key Responsibilities
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