Laboratory Configuration & QC Spec I

Do you have experience supporting clinical trials or are you working in a clinical research field? Have you thought about looking for ways to contribute in another area of research? How about becoming part of the ICON Laboratory Services (ILS) Central Laboratory Setup team where you’ll use your expertise to build trial specific study databases and all study related material such as Laboratory Manuals and study requisition forms. This position will give you a unique perspective into the ever important setup phase of a clinical trial including - being exposed to different study phases, study sizes and disease indications all while being a hands on participant in the building and creation of the trial.

About the Configuration/QC Specialist within ICON: 

The Configuration/QC Specialist will be support the Project Management Team (PM) in configuring and QC’ing new clinical studies in all ILS systems according to the specifications of the Client Laboratory Worksheet (CLW). You will create supporting documents for the site to facilitate proper specimen collection, coordinate packaging and shipping including visit requisitions, reference range tables, and study specific Lab Manuals and collection guides. Ensure information is clear and accurate and seek guidance on any parameters that need clarification.  

When updates or additions are requested the Configuration/QC Specialist will work with Leadership to determine whether or not those updates are warranted in the Lab Manual or Requisition Template and make those updates accordingly.

The Configuration/QC Specialist will perform new study configuration quality checks on all databases, internal forms and supporting documents to ensure high quality output and adherence to the CLW specs and provide technical support and guidance to Project Managers for all study configuration tasks.

Benefits of working at ICON:

We will provide our Specialist 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 possess a BS or equivalent combination of experience and education and an understanding of client and site needs is a plus. You will have one year experience in Clinical Trials, Laboratory or similar database configuration work with knowledge of basic computer programs such as MS Word, Excel, and Adobe Acrobat.   

Must have excellent written communication skills along with the ability to manage multiple projects and exhibit appropriate time management skills.

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