Job Information
ICON Clinical Research Clinical Data Quality Associate in Lenexa, Kansas
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.
ICON Clinical Research
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