Oruka Therapeutics Inc. is seeking a highly organized Trial Master File (TMF) Associate. This remote/hybrid role supports TMF management throughout the study lifecycle, ensuring documentation is complete, compliant, and inspection-ready.
You will partner with Clinical Operations, CROs, and vendors to maintain TMF health and drive quality improvements. Responsibilities include quality control, reconciliation, and audits preparation, with exposure to ICH-GCP, CDISC TMF, and FDA regulations.
#J-18808-LjbffrTMF Associate (Remote) – Quality & Compliance in menlo park at Unknown Company
This position is listed as full time and able to be worked remotely.