Scientific Affairs Specialist

About the job

At ICON its 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 touchpoint. In short to be the partner of choice in drug development.

Thats our vision. Were driven by it. And we need talented people who share it.

If youre as driven as we are join us. Youll be working in a dynamic and supportive environment with some of the brightest and the friendliest people in the sector and youll 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 ICONs 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

Please use the below link for job application and quicker response.

Remote Work :

No