Sr. Clinical Trials Associate

Role: Senior Clinical Trials Associate coordinating clinical research studies ensuring compliance with U.S. and international regulations. Responsibilities: support study setup, conduct, and documentation; liaise with vendors, sites, and cross-functional teams; track trial progress and ensure data integrity. Requirements: relevant bachelor's degree; experience in clinical trial coordination; knowledge of GxP and regulatory standards; strong organizational and communication skills. Preferred: familiarity with biopharma-specific software tools, experience with multi-regional trials. High-Value: regulatory compliance, international clinical trial coordination, GxP adherence. WorkSetup: not specified; likely office-based with potential remote elements.