Medical Device Study Start-Up Associate

Job Summary

Working remotely, the full-time Medical Device Study Start-Up Associate II will manage clinical trial site start-up activities, including regulatory document preparation and approvals, while ensuring compliance with legal and regulatory standards.

Key responsibilities

• Coordinate site regulatory submissions and essential document collection for clinical research sites
• Manage multiple sets of essential regulatory documents across various 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 clinical/scientific research experience, specifically in medical device study site start-up within the US
• Experience with clinical trial management systems and clinical document control systems
• Ability to multi-task in a fast-paced environment
• Clear and concise communication skills, both written and verbal