Site Activation Associate

Job Summary

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

Key Responsibilities

• Initiate and manage investigator site activities, including regulatory document submissions and informed consent form negotiations
• Oversee study regulatory maintenance activities and ensure compliance with training and country-specific requirements
• Communicate with sites to drive timelines and resolve issues while maintaining accurate trial performance records

Required Qualifications

• Bachelor's degree in a scientific or health-related field
• Two years of clinical research experience or relevant experience preferred
• Understanding of the clinical development paradigm and site activation processes
• Applied knowledge of project management processes
• Experience in a compliance-driven environment