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The Clinical Document Specialist, eTMF Operations, plays a crucial role in managing electronic Trial Master File (eTMF) documentation for Replimune's clinical trials. This position is responsible for the setup, maintenance, quality control, and archiving of eTMF documents, ensuring compliance with standard operating procedures and regulatory guidelines. The role requires collaboration across various teams to ensure that all necessary documentation is accurately collected and maintained, contributing to the overall success of clinical trials.