Clinical Data Analyst
About the role
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* Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance.
* As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
* Act as facilitator for Patient Centric Monitoring set-up, implementation and training within the cross-functional project team.
* *Track the implementation of Patient Centric Monitoring within the cross-functional project team.
* *Coordinate the set-up of the analysis platform, listing and working tools for Clinical Data Analysis.
* *Conduct risk indicator analysis, make independent decisions on analysis outputs and communicate them to the project team.
* *Support preparation, conduct and follow-up of the Quality Risk Review Meetings for effective communication with the project team and for effective resolution of study and site performance and quality issues.
* *Support cross-functional ICONik users with system set-up and use.
* Act as mentor for Central Monitoring team members.
* Support internal and external promotion of Patient Centric Monitoring and related systems.
* Travel (approximately 5%) domestic and/or international.
* Other duties as assigned.
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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IndustryContent type
BlogsPublish date
12/01/2025
Summary
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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IndustryContent type
BlogsPublish date
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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