About the job
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.
The Role:
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.
What you will need:
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
Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
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Remote - Middle East | Remote - Europe | Switzerland | Remote, USA | Remote |Bucharest :
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