About this role
Clinical Study Documentation Specialist at Caris Life Sciences. Location: Phoenix, Arizona, United States. Role: prepare documents, maintain files, coordinate submissions Requirements: Associates degree; 2 years IRB document submission; strong clinical research documentation; proficient in Microsoft Office and regulatory systems; strong organization; able to manage multiple studies; background checks required. Category: Research and Development (R&D) Seniority: Mid Level Tools: Microsoft Office, IRB portals, CTMS, Regulatory systems Commitment: Full Time Workplace: Onsite Languages: English