Must Have Qualifications: Bachelor's degree Ability to travel up to 80% Proficiency in Microsoft Office Applications (Word, Excel, PowerPoint, etc.) Knowledge of FDA Regulations (21 CFR 812) and ISO 14155 Nice to Have Qualifications: Experience with CTMS, RAVE, VeeVa Responsibilities: Monitor the progress of clinical trials at site level or headquarters, ensuring compliance with protocols, SOPs, GCP, and regulatory requirements. Enjoy the convenience of working remotely while having the opportunity to travel extensively across the United States, supporting groundbreaking clinical trials.