Minnesota Licensed Study Start Up Associate

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 essential regulatory documents and support informed consent form negotiations
• Develop relationships with clinical research sites 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 with medical device site start-up experience
• Ability to multi-task and work in a fast-paced environment
• Experience with clinical trial management systems and document control systems is preferred
• Must be comfortable working hybrid/on-site in Arden Hills, MN