Regulatory Specialist I

A company is looking for a Site Activation and Maintenance Associate I.

Key Responsibilities

Initiate and manage investigator site activities, including regulatory document collection and informed consent form customization

Oversee study regulatory maintenance activities and manage site changes, ensuring compliance with regulations

Drive timelines, communicate with sites, and resolve issues to maintain active collaboration and compliance

Required Qualifications

Bachelor's degree in a scientific or health-related field

Two years of clinical research experience or relevant experience preferred

Understanding of clinical development and site activation processes

Applied knowledge of project management processes

Experience in a compliance-driven environment