Jan 23, 2021
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Responsibilities: Responsible for the creation and approval of clinical label text for BMS studies through effective management of assigned projects. Generates label text in accordance with the clinical trial design and all relevant regulatory requirements for assigned projects. Liaises with responsible Trial Supplies Manager and regulatory approvers on aspects of clinical supplies packaging and labelling design and study requirements and resolves issues. Creates internal label proof(s). Ensures label proofs contain all information as identified in approved label...
Bristol Myers Squibb
New Brunswick, NJ, USA