Lab Analyst II (PRN/FT) - On-Site - US, Lenexa, KS
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Lab Analyst II to join our diverse and dynamic team. As a Lab Analyst II at ICON, you will be responsible for performing intermediate-level laboratory tests and analyses to support clinical research projects. You will contribute to the accuracy and reliability of laboratory data, while adhering to strict quality and regulatory standards, and playing a key role in the daily operations of the lab.
Title : Lab Analyst II
Location : On-Site (Lenexa, KS)
Job Type: PRN and Full-Time hours currently available.
The Role:
The Lab Analyst operates and maintains instrumentation and performs diagnostic clinical laboratory testing.
Routine sample processing with different analytical instruments and methodologies.
Interpret data and quality control data.
Identify and report irregularities identified with any aspects of work.
Recognize, exemplify, and adhere to ICON's values which center around our commitment to People, Clients, and Performance.
Ensures on-time task completion to support the overall goal of on-time study completion.
Perform assays for the routine batch analysis of physical/chemical analysis samples involving simple to complex analytical techniques. Perform laboratory work to GMP or GxP standard.
Work in compliance with study plans and validation plans and all relevant SOPs.
Document all work and results accurately, completely, and compliant with GMP or GxP regulations and SOPs.
Generate high-quality analytical results. Ensure the smooth transfer of data and participate in the evaluation and interpretation of data.
Operate general laboratory equipment and instrumentation systems and utilize automated data collection/reporting systems.
Maintain instruments.
Work in compliance with GMP or GxP.
Generate laboratory reports for work performed.
Perform routine maintenance and calibration of instrumentation.
To undertake other reasonably related duties as may be assigned from time to time.
To be successful in the role, you will have:
Bachelor's Degree - Preferably in a science-related field of study
Clinical laboratory experience is required.
Certified clinical laboratory scientist preferred.
Preferred Qualifications:
- MLS (ASCP) or MT (ASCP)
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
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