Clinical Research Associate, Sponsor Dedicated

Perform site monitoring visits, work with sites to adapt subject recruitment plan, administer protocol and related study training, and manage the progress of assigned studies.

Requirements

• Bachelor's Degree in scientific discipline or health care
• At least 2 years of on-site monitoring experience
• Good knowledge of clinical research regulatory requirements
• Good therapeutic and protocol knowledge
• Computer skills including proficiency in Microsoft Word, Excel, and PowerPoint
• Written and verbal communication skills
• Organizational and problem-solving skills
• Effective time and financial management skills