Study Start Up Associate II

Job Summary

A company is looking for a Study Start Up Associate II - Medical Device.

Key Responsibilities

• Coordinate site regulatory submissions and essential document collection for clinical research sites
• Manage multiple sets of essential regulatory documents and support negotiation of Informed Consent Forms (ICF)
• Provide updates on site start-up activities and ensure compliance with regulatory requirements

Required Qualifications

• Bachelor's Degree or equivalent combination of experience and education
• 2+ years of experience in clinical/scientific research and medical device site start-up
• Experience with clinical trial management systems and document control systems
• Ability to multi-task and work in a fast-paced environment
• Willingness to work hybrid/on-site in Arden Hills, MN