Clinical Research Associate

Job Summary

A company is looking for Experienced Gen Med CRAs to lead and support their Full Service Outsourcing team.

Key Responsibilities

• Monitor and manage all aspects of clinical study sites, including routine monitoring, close-out, and site management
• Ensure compliance with informed consent procedures and protocol requirements to protect study participants
• Conduct Serious Adverse Event (SAE) reporting and assist with training of new employees

Required Qualifications and Education

• University or college degree, or certification in a related allied health profession
• 1 - 3+ years of Clinical Monitoring experience
• Gen Med experience is desired
• Open to various hub locations across the US