Help early-stage clinical research teams identify and resolve quality risks before they disrupt studies or compromise patient safety. At Genentech, the work combines Good Clinical Practice guidance, trial oversight, quality-system improvements, staff training, and practical responses to compliance issues.
Candidates should bring a life-science or healthcare background, substantial drug-development and GCP quality experience, and the ability to translate regulatory expectations into clear guidance. Experience with early clinical trials, inspections, or vendor oversight is valued.
Posted annual base salary range: $141,100–$262,100; actual pay varies by qualifications and geographic location.
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