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Quality Process Specialist I

042373_2

About the role

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At ICON, it's our People that set us Apart" 

ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies 

ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart. 


JOB FUNCTIONS/RESPONSIBILITIES

(List statements in bullet format. Put an asterisk* next to each essential function. The definition of an essential function is included in the Job Description Form Guidelines within iDoc)

• 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.

• Travel (approximately 5%) domestic and/or international, as applicable

• Follow standardized procedures and practices

• Understanding of purpose, objective, practices and procedures of the job role

System and General Administration:

• Capable and knowledgeable of system functionality and requirements pertaining to job role

• Provide support, as needed, to global Quality Assurance Department

• Assist with the continuous development of processes to support the Quality Assurance Department

• Serve as backup to all other QA process specialists (globally) as necessary

• Other duties as required

• Keep the person to whom the QA Process Specialist reports informed of any quality issues within the department/office which require attention

SUPERVISION

(List statements in bullet format. Put an asterisk* next to each essential function.)

• Non-supervisory role

• Able to work under moderate supervision and effectively manage own workload

List #1

Day in the life

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Leading Through Change: Zhong Yao's Journey at ICON in China

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Our People

Content type

Blogs

Publish 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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From culture to collaboration, Zhong Yao explains how ICON China delivers quality clinical trials, and empowers local talent.

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How Data Moves Through a Clinical Trial

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Industry

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Publish date

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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Discover how data flows through a clinical trial and learn where your skills could fit within clinical research.

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Quality and Compliance - A Plain Language Guide

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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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A clear, practical introduction to quality and compliance for those starting a career in clinical research.

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