Study Delivery Sr Associate

The Study Delivery Senior Associate provides essential global study management support to clinical study teams, ensuring timely, high-quality, and compliant study execution. They partner with Study Managers to deliver start-up and conduct activities, own specific study tasks and support risk monitoring and issue management, escalating early warning signals with proposed solutions to relevant stakeholders.

Requirements

• Master’s degree OR Bachelor’s degree and 2 years of clinical execution experience OR Associate’s degree and 6 years of clinical execution experience OR High school diploma / GED and 8 years of clinical execution experience
• 3 years’ work experience in life sciences or medically related field, including 1 year of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
• Experience working on global clinical trials
• Competencies: Strong collaborative and effective communication skills within a team environment. Understands importance of accuracy in documentation, data tracking, and compliance checks. Identifies discrepancies and escalates appropriately.
• Experience with using MS Word, Excel, PowerPoint, and other relevant software for documentation, data management, and trial support

Benefits

• Medical, Dental, Vision
• 401(k) Savings Plan
• Flexible Spending Account
• Stock Purchase Plan
• Paid Time Off
• Life Insurance
• Wellness Programs