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The role will be responsible for independent drug monitoring for assigned studies. This responsibility will include end to end ownership for the trial, from the initial set up and drug blinding activities, to ongoing monitoring of studies, and any duties needed for the successful closure of said trials. This role will accelerate any issues found during monitoring and will work to resolve said issues. This role will be responsible for keeping the study team, sites, and all other applicable stakeholders well informed of the progress of drug monitoring as well as communicating any compliance issues. Further duties include developing documents and materials...