Description
Arcus Biosciences is hiring a Senior Clinical Document Specialist for a six-month full-time remote contract in the United States. The role manages and maintains Trial Master File (TMF) documents for clinical programs, supports TMF content owners and study teams, performs document collection, review, classification, quality control, reconciliation, and eTMF maintenance, and supports audit and inspection readiness. The position requires clinical trial experience, knowledge of ICH/GCP and regulatory guidance, familiarity with Veeva Vault and DIA, and strong organizational and communication skills.
