Clinical Trial Manager (CTM)

Role: Senior Clinical Trial Manager responsible for end-to-end management of assigned clinical trials in biopharma, with a focus on drug development processes. Responsibilities: oversee trial operations, manage CRO/vendor relationships, ensure compliance with GCP, FDA, EMA, and ICH regulations; collaborate with Data Management on CRFs and data deliverables; coordinate with study teams, site investigators, and stakeholders; monitor enrollment, trial progress, and budgets; prepare for audits and inspections; identify risks and implement solutions. Requirements: B.S. in biological sciences or related field; 5+ years of industry experience managing clinical trials independently; strong knowledge of regulatory guidelines; excellent communication, organization, and problem-solving skills; ability to travel (~25%). Preferred: experience in oncology, immunology, or inflammatory diseases; familiarity with targeted protein degradation modalities; experience in early-phase (Ph1-3) trials. HighValue: full trial lifecycle ownership, vendor management, regulatory compliance, and cross-functional team leadership in a fast-paced, innovative biopharma environment. Work Setup: onsite in Brisbane, CA; travel required.