Clinical Data Quality Associate
- Lenexa
- Clinical Data Management
- ICON Full Service & Corporate Support
- Office Based
About the role
This vacancy has now expired. Please click here to view live vacancies.
CDQA – Lenexa, KS:
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
What will you be doing?
- Quality Check source documents against Good Documentation Practices and study protocols
- Perform entry of data from source documents into Case Report Form database
- Organize and maintain subject charts for review by clinic staff and other study team members
- Communicates identified errors and supports clinic staff to resolve in a timely manner
- Collaborates with study team members (e.g. Data Managers, Study Managers, Study Monitors) to navigate data quality issues and meet study timelines
- May assist with developing new work methods for data entry and QC of study documentation
Qualifications:
- Read, write, and speak fluent English; fluent in host country language required
- High School Diploma, G.E.D., or secondary vocational education required
- 1-2 years work experience in quality control, data entry, or clinical research preferred
Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
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. See all locations Learn more about Our Culture at ICON
Day in the life

Teaser label
Our PeopleContent type
BlogsPublish date
10/02/2023
Summary
An Evolution of Progress and Success: Zashan's story a Clinical Research Associate (CRA) Having a satisfying career involves finding a company that prioritizes progress, improvement, and chances f

Teaser label
Our PeopleContent type
BlogsPublish date
05/19/2023
Summary
Skip to SAS Programming jobs What does a SAS programmer do? SAS programmers write, alter, and test the scripts and code that make it possible for applications to execute work from requir

Teaser label
A Day In The LifeContent type
BlogsPublish date
04/21/2023
Summary
From Clinical Trial Assistant to Clinical Operations Manager, Adrienne Purdy shares her journey.Tell us about you role and what you do at ICON? I have been at ICON since 2013 and I have been growing
by
Adrienne Purdy
Similar jobs at ICON
Salary
Location
Poland, United Kingdom
Department
Biometrics Roles
Location
Poland
UK
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Data Management
Clinical Data Scientist Lead
Clinical Systems
Data Standards Consultant
Job Type
Permanent
Description
We are currently seeking a Senior Medical Coding Specialist to join our diverse and dynamic team. As a Senior Medical Coding Specialist at ICON, you will play a key role in ensuring accurate and consi
Reference
2025-120188
Expiry date
01/01/0001
Author
Jacek JaworskiAuthor
Jacek JaworskiSalary
Location
United Kingdom
Department
Biometrics Roles
Location
UK
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Biometrics Portfolio
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech
Reference
2025-120855
Expiry date
01/01/0001
Author
Niki ScottoAuthor
Niki ScottoSalary
Location
Bangalore
Department
Biometrics Roles
Location
Bangalore
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Biometrics Portfolio
Job Type
Permanent
Description
The role involves being a Senior Lead clinical data science programmer in the Clinical Data Management area, focusing on enhancing data review and cleaning processes with innovative reports. It entail
Reference
2025-120626
Expiry date
01/01/0001
Author
Abhisikta MishraAuthor
Abhisikta MishraSalary
Location
Taipei
Department
Biometrics Roles
Location
Taipei
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Biometrics Portfolio
Job Type
Permanent
Description
As a Statistical Programmer, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-120472
Expiry date
01/01/0001
Author
Huixin "Stella" SongAuthor
Huixin "Stella" SongSalary
Location
Mexico, Mexico City
Department
Full Service - Development & Commercialisation Solutions
Location
Mexico City
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Data Management
Job Type
Permanent
Description
Clinical Data AnalystWhat you will be doing:The Clinical Data Analyst supports Imaging Science, Project Management, and Radiology in the review and approval of image analysis for data delivery.Manage
Reference
JR131874
Expiry date
01/01/0001
Author
Daniela GuerreroAuthor
Daniela GuerreroSalary
Location
Argentina
Department
Biometrics Roles
Location
Argentina
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Data Management
Clinical Data Scientist Lead
Clinical Systems
Data Standards Consultant
Job Type
Permanent
Description
(Talent pool) As a Clinical Data Coordinator you will play a key role in improving the lives of patients by accelerating the development of our customers drugs and devices through innovative solutions
Reference
2025-116863
Expiry date
01/01/0001
Author
Tulio SanquizAuthor
Tulio Sanquiz