Associate Clinical Trial Manager

Are you a Senior CTA or an In-House CRA seeking career advancement? If so, we currently have multiple CTMa ( Associate Clinical Trial Manager/Junior CTM ) roles in the SF Bay Area. Most are hybrid, so we seek *** LOCAL BAY AREA CANDIDATES ONLY

Duties Include: Support Clinical Study Management team members in the day-to-day execution of global clinical trials Perform vendor management TMF Management Site Management Maintain study timelines, risk logs, and action trackers Manage clinical site budget tracking, site/vendor invoices, and vendor communication Use clinical systems such as CTMS, EDC, and eTMF to resolve data queries and manage clinical trial data Participate in the design of study-related documents (clinical protocols, case report forms (CRFs), site study manuals, project tools, monitoring plans, tracking tools, and informed consent forms (ICFs)) Apply your basic knowledge of ICH-GCP and FDA regulatory requirements to ensure your clinical studies are compliant Maintain tracking systems (e.g., site status, enrollment metrics); assist with study start-up activities (e.g., site feasibility, essential document collection). Mentor and support CTAs.