Senior Clinical Trials Associate

To support the Clinical Operations team, the full-time salaried Senior Clinical Trials Associate will independently coordinate clinical trial activities from start-up through close-out, ensuring compliance with ICH/GCP guidelines and operational excellence while working remotely. Key Responsibilities Independently support and coordinate clinical trial activities from start-up through close-out Serve as primary owner of Trial Master File (TMF) quality, completeness, and inspection readiness Collaborate with CROs, vendors, and sites to ensure study milestones and deliverables are met Required Qualifications Bachelor's degree in a scientific or healthcare-related field preferred; equivalent experience considered 2-3+ years of clinical operations experience in biotechnology, pharmaceutical, or CRO settings Experience supporting Phase 1-3 clinical trials Hands-on experience with TMF management and clinical systems (eTMF, CTMS, EDC) Working knowledge of ICH/GCP and applicable regulatory requirements