At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.

Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That’s our vision. We’re driven by it. And we need talented people who share it.

If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

To provide technical / scientific support to both internal and external clients. To assist in the delivering and monitoring of consistent deliverables for Global Scientific Affairs.

• Maintain and configure testing and assay summary information in the Test Master application of the ICOLIMS system.

• Configure test codes within the STARLIMS system.

• Assist all other ICL departments with Global Scientific Affairs related issues and questions.

• Utilize the internet, journals, internal validation documentation, etc. to update specimen requirements, stability, and transport information within departmental databases.

• Follow SOPs relevant to Global Scientific Affairs issues.

• Attend meetings with both internal and external clients on behalf of Global Scientific Affairs.

• Provide notifications and technical documentation to the Global Validation Department and ultimately Global Client Services.

• Maintain CLSI documents library.

• Performs additional relevant responsibilities as requested by management.

• Recognize, exemplify and adhere to ICON's values, which centers around our commitment to People, Clients and Performance.

• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.

• BS Degree in Medical Technology, preferred.

• Experience in Analytical Platforms such as Siemens, Roche, Abbott, Beckman is preferred.

• More than 5 years relevant experience

• Knowledge of clinical laboratory concepts and terminology

• Knowledge of Microsoft Word and Excel