ICON Clinical Research

Validation Analyst II, Labs

Location
Oyster Bay,dublin
Salary
Competitive
Posted
22 Feb 2021
Closes
24 Mar 2021
Ref
1JR068614
Discipline
R & D , Laboratory
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
Are you a Medical Technologist or Biomedical Scientist with experience providing solutions for clinical lab testing? If so, learn how you can lead all responsibilities surrounding the performance of analytical validations within ICON Laboratory Services (ILS).

About the Laboratory Validation Analyst role within ICON:

The Laboratory Validation Analyst will assist in the design and documentation of validation plan, correlation or stability plans, prepare results analysis reports, and prepare accuracy, precision, correlation, or stability samples for validation studies.

The Laboratory Validation Analyst will be responsible for the performance of required manual procedures and operation of automated instrumentation under supervision of the Manager or Laboratory Director as necessary and maintain a readily accessible, up to date electronic library of completed validation, correlation, or stability study statistical experiments. When required, the Validation Analyst will also import data into a statistical analysis tool such as EP evaluator or equivalent.

Benefits of working at ICON:

We will provide our Laboratory Validation Analyst with the resources to be successful in supporting their line of business. In addition, we offer a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation, and an annual incentive plan to reward performance.

To succeed you will need:

You will need to possess Bachelors or Master's degree in Medical Technology, Biomedical or equivalent science and have a Minimum 5 years' experience in Medical Technology/Clinical Lab Sciences field. Working experience in assay validation in a clinical laboratory setting is advantageous. Good analytical and troubleshooting skills. Self-starter with new projects, while following SOP guidelines, good researching capability, ability to work independently and manage multiple projects simultaneously, ability to think critically and creatively to identify and solve scientific problems, strong interpersonal skills and excellent oral and written communication skill a must, and experience working in a highly collaborative and motivated working environment.

Knowledge of or ability to learn CAP, NYS, and CLSI regulatory guidelines.

We invite you to review our opportunities at www.iconplc.com/careers .

What's Next?

Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment

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