Clinical Trial Manager

Position SummaryWe are seeking a highly motivated Clinical Trial Manager (CTM) to support the planning, execution, and oversight of global clinical trials. This individual will work cross-functionally with internal teams, CROs, vendors, and study sites to ensure studies are conducted in compliance with protocol requirements, GCP, regulatory guidelines, and company timelines.The ideal candidate will have experience working within a small, fast-paced biotechnology company environment, managing global clinical trials across multiple regions, including Asia-Pacific (APAC), and possess therapeutic area experience in inflammation and/or immunology.This will be a hybrid on-site position in San Diego. If outside of the San Diego area, open to remote candidates but must be located on the west coast. Key ResponsibilitiesManage day-to-day operational execution of global clinical studies from study start-up through closeout.Serve as the primary operational lead for assigned clinical trials, ensuring milestones, timelines, and deliverables are achieved.Oversee CROs and vendors, including performance management, issue resolution, and quality oversight.Collaborate with Clinical Operations leadership, Clinical Development, Data Management, Biostatistics, Medical Monitoring, Regulatory Affairs, and other functional groups.Lead study team meetings and provide regular updates on study progress, risks, and mitigation plans.Monitor study enrollment, data quality, protocol compliance, and site performance metrics.Support development and review of study-related documents including protocols, informed consent forms, study plans, and operational manuals.Manage study budgets, forecasts, and vendor invoices.Ensure inspection readiness and compliance with ICH-GCP, SOPs, and applicable regulations.Support global site management activities and coordinate across North America, Europe, and APAC regions.QualificationsBachelor's degree in Life Sciences, Nursing, or a related scientific discipline.4–8 years of clinical research experience with at least 2 years of study management or Clinical Trial Manager experience.Experience working in a small or emerging biotechnology company environment.Experience managing global clinical trials, including oversight of sites and vendors within APAC countries.Therapeutic area experience in inflammation, immunology, autoimmune diseases, or related indications.Strong understanding of ICH-GCP guidelines and global clinical trial regulations.Demonstrated experience managing CROs and external vendors.Excellent project management, organizational, and communication skills.Ability to thrive in a dynamic environment and manage multiple priorities simultaneously.