Minnesota Licensed Study Start Up Associate

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)

Ensure compliance with regulatory requirements and provide updates on site start-up activities

Required Qualifications

Bachelor's Degree or equivalent combination of experience and education

2+ years' experience in clinical / scientific research and medical device site start-up

Ability to multi-task in a fast-paced environment

Experience with clinical trial management systems and document control systems

Comfortable interacting with clinical research site personnel via phone and email