Site Identification Lead
About the role
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Do you have Global/Regional Study Start Up Site Identification and are now looking to further develop, implement and execute Site identification plans.
As Site Identification Lead you will be accountable for the development of Site Identification Plans. Working with the Study Start up, PM and CTMs on the study to ensure delivery of the study start up timelines in terms of initiated sites and First Patient In (FPI) milestones. Ensuring all sites proposed for selection are of a high quality standard and meet all site profile, due diligence and protocol specific site requirements. As a subject matter expert in Site Identification/Selection process for internal and external customers alike and to provide input to Team members, Project teams, Business Development and to Sponsors.
You will need Global Site Identification experience, leading sponsor initiatives such as kick-off meetings, bid defenses, project update and status calls, and other communications. We ask that you have a Bachelor’s degree, project and client interaction skills, and experience leading Site Identification activities globally in a clinical research environment.
As a Site Identification Lead, you would advance clinical trial Site identifications activities by understanding the client objectives and assist in the development of the Site Identification Plans through leading a team of Site Identification Specialists (SIS’s) who have responsibility for Site Identification. The successful candidate will show capability in the areas of clinical trial operations, meeting Site Identification and ICON guidelines, and displaying project management skills to optimize performance and collaboration to ensure successful study outcomes.
To succeed you will need a Bachelor’s Degree preferably in life sciences with great project management skill set and understanding of Site identification processes in many different countries along with experience in a clinical research environment (preferable focusing on Site Identification Activity).
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
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Our PeopleContent type
BlogsPublish date
12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
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12/01/2025
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How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
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11/28/2025
Summary
Quality and Compliance for New Entrants: A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job
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