Study Delivery Associate

The Study Delivery Associate provides essential administrative and operational support to clinical trial management activities, including maintaining accurate and timely data, supporting study training, and executing standardized processes related to clinical trial coordination, document and system management.

Requirements

• Bachelor's degree OR Associate's degree and 4 years of clinical execution experience OR High school diploma / GED and 6 years of clinical execution experience
• 2 years' work experience in life sciences or medically related field, including 1 year of biopharmaceutical clinical research experience
• Expertise in clinical trial processes, operations, and oversight in biotech, pharmaceutical, or Contract Research Organization environments
• Strong skills in using MS Word, Excel, PowerPoint, and other relevant software for documentation, data management, and trial support

Benefits

• Career development opportunities
• Competitive salary and benefits package