Study Delivery Associate

The Study Delivery Associate provides administrative and operational support to clinical trial management activities, ensuring regulatory compliance and executing standardized processes. The role involves maintaining accurate data, supporting study training, and promoting expertise and consistency across studies.

Requirements

• Bachelor's degree in a related field
• 2 years' work experience in life sciences or a medically related field
• 1 year of biopharmaceutical clinical research experience
• Experience working on global clinical trials

Benefits

• Equal Opportunity Employer
• Reasonable Accommodation for Individuals with Disabilities