To support clinical trials, the full-time Regulatory Analyst I will prepare, submit, and maintain regulatory documentation from study start-up through closure while working remotely. Key responsibilities Facilitates the preparation of regulatory documentation for study submissions to various boards and sponsors Provides regulatory support for multiple clinical trials, ensuring compliance with applicable regulations Generates and updates essential regulatory documents, including consent forms and protocol packages Required qualifications Bachelor's Degree in a relevant field Minimum one year of relevant experience in compliance, research, or clinical settings Knowledge of federal, state, and local regulations related to clinical trials Proficiency in Microsoft Office and experience with regulatory documentation processes Familiarity with clinical research protocols and informed consent documents