rgarza on April 30th, 2010
Specific responsibilities include study protocol development, collection of data through patient evaluation, statistical analysis and interpretation of the data, and presentation of results in written and oral format to project development teams. This must be done while complying with study protocols, departmental SOP’s, FDA regulations, and ICH/GCP guidelines.
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rgarza on April 30th, 2010
Clinical Research Scientist has overall responsibility for scientific clinical trials of investigational and approved contact lenses and/or contact lens care systems.
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