Project Coordinator
About the role
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ICON Clinical research is looking for a Project Coordinator to be based in Chennai. As a project Coordinator you will
- Provide support to the Project Management Department and assistance to Project Manager(s) in completion of all required tasks to meet departmental and project goals.
- Support the cross-functional teams regarding development and maintenance of the trial master file and study specific documentation.
- Set up, organize, track and maintain clinical study and project documentation both hardcopy and electronic (e.g. Main Study Files, CRFs, etc.) including document receipt and review, scanning and indexing, quality control, copying, filing, preparation for internal/external audits, final reconciliation and archival.
- Assist in quality control audits of clinical study and project documentation (e.g. Main Study Files, CRF Files, Monitoring Files, etc.)
- Assist with Investigative site and vendor contract execution, if required.
- Assist with submissions to the Independent Ethics Committee and Hospital Ethics Committees, if required.
The ideal candidate would have good communication skills and a life science degree is prefered
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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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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