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Salary
$47k – $59k per year
Location
In office (New York)
Seniority
Junior · 1+ year exp
Visa
Sponsors visas in United Kingdom, Ireland; no register of this country names it
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 12, 2026. First seen by Alion on Nov 11, 2026. ICON scores A on the Alion truth index.

Overview
Company
Impact
Profile match
ICON is an Irish clinical research organisation that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies, from early-phase trials to late-stage studies, laboratory services and real-world evidence. Founded in 1990 and listed on Nasdaq, it operates worldwide with tens of thousands of employees. The company is headquartered in Dublin, Ireland.
Quality Control Analyst I (QC), Bioanalytical, Clinical Research (CRO), Full time, M - F, Whitesboro, New York (NY)

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.

We are seeking a Quality Control Analyst I (QC) to support the Bioanalytical Laboratory and Project Management Teams at ICON's Whitesboro, New York site. The Quality Control Analyst I (QC) will perform quality control (QC) inspections to identify deficiencies and communicate with internal and external teams to resolve deficiencies in a timely manner.

The role:

  • Perform quality control (QC) inspections to identify deficiencies in sample handling/preparation, reagent preparation, laboratory methods, notebooks, raw data, and report tables.
  • Review study materials for compliance with the protocol, standard operating procedures (SOPs), and applicable regulations.
  • Perform verification of operational activities including review of notebooks, raw data, and report tables.
  • Employ rapid feedback loop to resolve deficiencies found during QC inspection. Ensure subsequent correction(s) are made.
  • Assist in the implementation of the quality management system, including both corrective and preventive actions.
  • Maintain accurate and complete records and ensures QC documentation is incorporated into appropriate study files.

You will need:

  • BS or equivalent combination of experience and education and an
  • Understanding of client and site needs, and external regulatory requirements
  • 1+ year's experience in a laboratory or research environment, highly preferred
  • Immunoassay exposure, great to have
  • Self-starter with track record of well-developed learning strategies.
  • Must be self-motivated and work well with various internal groups.

#LI-KM3

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

$46,864.00-$58,580.00

Are you a current ICON Employee? Please click here to apply

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