State Licensed Senior Clinical Research Associate

Job Summary

To support clinical activities at multiple study sites, the full-time remote State Licensed Senior Clinical Research Associate will manage monitoring tasks and foster strong relationships with colleagues in the healthcare industry.

Key responsibilities

• Manage clinical activities and monitoring at various study sites
• Develop and maintain productive relationships with site staff and stakeholders
• Ensure compliance with regulatory requirements and study protocols

Required qualifications

• At least 5 years of regional field monitoring experience
• State licensure as a Clinical Research Associate
• Experience in the pharmaceutical, biotechnology, or medical device industries
• Strong understanding of clinical trial processes and regulations
• Ability to work independently in a remote environment