Clinical Research Associate

Job Summary

To support genetic research initiatives, the full-time Clinical Research Associate will manage study protocols, coordinate data collection, and ensure compliance with regulatory standards while working remotely in Minnesota and Wisconsin.

Key responsibilities

• Manage and oversee study protocols and timelines for genetic research projects
• Coordinate data collection and ensure accuracy and compliance with regulatory requirements
• Collaborate with cross-functional teams to facilitate project progress and reporting

Required qualifications

• Bachelor's degree in a relevant scientific field
• Experience in clinical research, particularly in genetics
• Knowledge of regulatory guidelines and compliance related to clinical studies
• Proficiency in data management and analysis tools
• Ability to work independently and remotely while managing multiple projects