Oversees COH research protocols, sponsored research protocols, and commercial protocols for CAR T Cell program and other cellular therapy programs including genetically modified CD34 cells and cytotoxic lymphocytes. This person is responsible for maintaining current versions of lab protocols, attending site visits and other related meetings, writing SOPs, training, updating protocol binders with new versions and patients on study, corresponding with protocol personnel regarding study-related issues, receipt of products and infusion orders, and product quality certificates. Prepares and participates in audits conducted by protocol personnel, and assumes other related activities as delegated by the
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