Data Configuration Specialist
Pharma
Job description
Eurofins Scientific is an international life sciences company, which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the leading global emerging players in specialty clinical diagnostic testing. In 2020, Eurofins generated 4.2 billion Euro proforma turnover in 800 laboratories across 50 countries, employing about 50.000 staff. Eurofins Technologies is a new International Business Line (IBL) within the Eurofins Group focused on the development, manufacturing and marketing of bioanalytical technologies and diagnostic test kits in particular. The business if primarily focused on solutions in Food Safety and Environmental Safety but has recently expanded into Animal Health and Clinical Diagnostics. Eurofins Technologies serves both external customers (industrial laboratories, governmental laboratories, service laboratories) as well as customers within the Eurofins Group. Purpose of the Job and Expected outcome  Configure the Laboratory Information Management System LIMS dbase throughout the duration of the study inline with the Clinical Protocol, performing appropriate QC controls according to global procedures and agreed specifications. Ensure that the electronic data generated is transferred to the customer as per the Data Specifications.  Key Accountabilities  Data Configuration Specialist supports activities for studies during all stages in such a way that:  Tasks have been carried out independently, and the status or result is communicated back to all relevant parties.   Database to be set up as per client protocol.   Configure the study-specific requirements in the (LIMS) for central laboratory testing in clinical trials  (e.g. visit schedule, testing panels and flagging).   Collaborate with project management, laboratory, IT and clients.   Is aware of key study milestones and prioritizes study activities to achieve the timelines.   Format the Database as per desired type of data.   Ensure that LIMS and other systems are correctly configured in line with study Priming Document.   Maintain complete and current version controlled Data Study Files.        Experience:   Minimum 2 years work experience.  Education:  Bachelor degree in a related field.    Other Proactive: is flexible, anticipates fast and accurate on problems, sets the right priorities and organize their own work by choosing an approach that leads to the right solution. Professionalism: mastered knowledge and expertise regarding the work, works independently according professional standards. Quality oriented: works according the procedures and identifies matters that are not regulated and that need a decision of ‘a more experienced employee '. Monitors the implementation of the work. Customer driven, strong communication skills. Excellent command of the English language, spoken and written, knowledge of other languages is a plus. PERSONAL CHARACTERISTICS Eurofins has a culture of high professional standards, with strong processes, and an eye for details. Candidates will need to be fully aligned with this culture, which implies a structured and analytical approach, pragmatism, and modesty.   EVOLUTION: In a fast-growing group, successful leaders are frequently being offered increased areas of responsibility (subject to geographic mobility). Gender: No Preference.
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