Site Management Associate

Job Summary

A company is looking for a Site Management Associate I.

Key Responsibilities

• Assist in monitoring clinical trial sites for adherence to study protocols and regulatory requirements
• Support site management activities, including documentation preparation and data entry
• Collaborate with cross-functional teams to address site-related issues and maintain accurate records

Required Qualifications

• Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research
• Some experience in clinical research or site management is preferred but not mandatory
• Basic knowledge of clinical trial processes and regulatory requirements is a plus
• Strong organizational skills with the ability to manage multiple tasks effectively
• Excellent interpersonal skills and ability to work collaboratively within a team environment