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The role requires the ability to be able to build out a database appropriate for different types of genomic data.
Looking at the results of 1st and 2nd stage summary and the gene expression levels.
This would tie in the data from experimental sides, predictions and transcriptions. Also read outs for the genomics bench side. This would be a small database.
The ideal candidate will have experience in designing, building and updating clinical trial study databases according to specifications.
Providing technical solutions for ad-hoc study requirements, as well as leading their development
Inputting into the development of database and software solutions
Working closely with lead data managers to lead study database programming elements
Providing support and technical assistance for internal and external reported issues
Performing, guiding and facilitating functional testing of study specific software enhancements.
PhD in Computational Biology would be ideal but a Masters in some form of computational science will also be considered.