Site ID Specialist I
About the role
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- Work with the Site ID Lead to ensure knowledge of the goals, scope and requirements of the site ID project (e.g. number of sites required/country, number of positive responses required etc.) and ensure that high quality results are delivered.
- Identify study investigators/ sites for potential study participation, both from the database and other potential sources such as local intelligence/internet etc. Ensure all newly identified sites are data based appropriately, checked for quality status and are fully processed.
- To contact and build relationships with study investigators/ sites and networks in assigned areas (e.g. region(s), countries / countries or therapeutic area) for the conduct of feasibility and potential study participation.
- To liaise with country managers to gather country specific evidence to support site identification, e.g. site list review, country specific profile of sites, standard of care
- To ensure that all data collected in the conduct of site identification or site related country feasibility fully documented and kept up to date in ICON’s systems in order to build knowledge and intelligence
- To ensure appropriate procedures are followed, whether Sponsor specific or according to ICON SOPs
- Ensure appropriate follow through with sites on any inconsistencies in data provided for analysis and to chase outstanding feasibility data to ensure a complete data set.
- To contact investigators, local ICON employees and collect data to support country choice in the conduct of feasibility assessments.
- To become a country expert on the investigator profile, healthcare setting, standard of care to ensure the best sites are approached for projects.
- To liaise cross-functionally with other departments such as Study Start Up, CRA management to to support local data collection
- Be an expert on how to interact with sites and obtain relevant information to support feasibility and site identification.
- Use knowledge and experience to build efficiency in the process and consistently deliver high quality investigators, sites, and other data to the Functional Lead for your feasibility projects.
- Bachelor’s degree, or local equivalent, in a life science, communication, and/or scientific discipline.
- Alternatively a shorter degree would be considered if the above experience was met
- 2 or more years of experience, in a health care or a clinical research environment
- Intermediate skills in MS Word, Excel and PowerPoint, advanced skills are preferred, particularly for Excel
- Highly developed organizational and analytical skills, with the ability to prioritize time-sensitive tasks and work independently
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