ICON
Configuration & QC Specialist I
NY, Farmingdale, United States · Work style not stated · Full time
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About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerICON
- LocationNY, Farmingdale, United States
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
Configuration & QC Specialist I
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
Configuration & QC Specialist I
Hybrid, Remote, or Office-Based | United States
Help Advance Clinical Research
Join ICON Central Laboratories and play a key role in supporting clinical trials that help bring innovative treatments to patients worldwide. As a Configuration & QC Specialist I, you'll help configure and validate clinical trial laboratory databases, ensuring accuracy, quality, and compliance while partnering with cross-functional teams in a collaborative, fast-paced environment.
Show full description
Location: This position may be hybrid, fully remote, or office-based depending on the selected candidate's location and business needs. Eastern Time Zone (EST) candidates are preferred.
What you will be doing
- Support the configuration and setup of clinical trial laboratory databases (LIMS).
- Perform quality control reviews to ensure data accuracy and compliance.
- Investigate and resolve configuration discrepancies.
- Partner with Project Managers, Setup Specialists, and Scientific Affairs teams.
- Maintain accurate documentation and support project deliverables.
- Contribute to continuous improvement initiatives.
What You'll Bring
- Strong attention to detail and analytical skills.
- Excellent communication and organizational abilities.
- Ability to manage multiple priorities in a fast-paced environment.
- Proficiency with Microsoft Office, including Excel.
- Ability to work independently and collaboratively.
Preferred Qualifications
- Experience in configuration, quality control, quality assurance, or data management.
- Experience in healthcare, clinical research, or other regulated environments.
- Familiarity with validation, documentation, and quality processes.
Why ICON?
At ICON, you'll be part of a global team dedicated to advancing clinical research and improving patient outcomes while enjoying flexibility, collaboration, and opportunities for professional growth.
#LI-HD1
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Salary Range
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At a glance
- Employment typeFull time
- Employer posted
- Added to ROLIVA
- Last checked
Skills in this posting
Skills ROLIVA found in the employer’s own description above. A mention is not a requirement.