Flow Cytometry Medical Technologist II — Central Lab Impact

ICON Clinical Research; Ireland; On-site; EUR 44,000 - 64,000; Full time

Benefits offered by this job

Health insurance

Annual leave entitlements

Life assurance

Retirement planning options

Global Employee Assistance Programme (

LifeWorks

Job summary

ICON plc in Dublin, Ireland, is seeking a Medical Technologist II to join the Central Laboratory and Flow Cytometry Department, ensuring testing of clinical trial samples and reporting results in line with quality standards and SOPs.

You will work with a diverse team, apply strong interpersonal and communication skills, and contribute to process improvements, maintaining accurate documentation and adherence to GLP/GCP expectations in a fast-paced environment.

Qualifications

• Bachelor's degree in medical laboratory science or Life Sciences.
• 1+ years' experience in a Flow cytometry laboratory.
• Experience with CTC analysis, PBMC isolation and DNA extraction is desirable but not required.
• Strong interpersonal and communication skills; ability to work independently and in a team.

Responsibilities

• Test clinical trial samples for flow cytometry assays.
• Adhere to ICON's Quality Control SOPs and document results accurately.
• Perform equipment checks, maintenance, and QC per guidelines.
• Review test requests for errors and ensure patient identification accuracy.
• Participate in proficiency testing and maintain assay tracking records.
• Support process improvements and collaborate with cross-functional teams.

Skills

Flow cytometry

Interpersonal skills

Communication

Laboratory operations

Multitasking

Problem solving

Teamwork

Education

Bachelor's degree in medical laboratory science or Life Sciences

Tools

Central Laboratory equipment

Flow Cytometry instruments

Job description

ICON plc in Dublin, Ireland, is seeking a Medical Technologist II to join the Central Laboratory and Flow Cytometry Department, ensuring testing of clinical trial samples and reporting results in line with quality standards and SOPs.

You will work with a diverse team, apply strong interpersonal and communication skills, and contribute to process improvements, maintaining accurate documentation and adherence to GLP/GCP expectations in a fast-paced environment.