Study Start Up Associate

Job Summary

Working remotely, the full-time Study Start Up Associate will manage clinical trial site start-up activities, including regulatory document preparation and approval, while collaborating with clinical teams to ensure compliance with service agreements and regulations.

Key responsibilities

• Coordinate site regulatory submissions and essential document collection for clinical research sites
• Manage multiple sets of essential regulatory documents across several studies and divisions
• Develop relationships with clinical research sites to support informed consent form negotiations and customizations

Required qualifications

• Bachelor's Degree or equivalent combination of experience and education
• 3+ years of experience in clinical research with a focus on medical device study site start-up
• Experience with clinical trial management systems and document control systems
• Ability to multi-task in a fast-paced environment
• Strong communication skills for interaction with clinical research site personnel