Clinical Site Associate

ICON · Tokyo, Japan +1 more

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Clinical OperationsFull-timeCompany career page

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Role summary

Clinical Site Associate role supporting site management and scientific operations for clinical trials at ICON. Responsibilities include site activation, document management, communications coordination, and logistics support to ensure trials run efficiently and compliantly.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-04 (originally posted 2026-10-04). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

Bachelor's degree in life sciences, healthcare, business, or related field
Initial experience in clinical research, administration, or regulated environment preferred
Strong organizational skills managing multiple tasks and deadlines
High attention to detail in documentation and data entry
Proficiency with MS Office and electronic systems/databases
Effective written and verbal communication skills
Ability to travel approximately 10% as required

What you'll be doing

Support site activation including document collection, review, and tracking of approvals
Maintain site information and status in clinical trial management systems
Assist CRAs with site communications and resolution of site-level queries
Coordinate logistics for site visits, scheduling, and documentation
Ensure accurate filing and maintenance of essential documents for audits

Privacy & handoff

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What RoleLantern checked

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Date posted1 day ago

Last source checkToday

Salary listedNeeds clarity

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