Regulatory Analyst I

Job Summary

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