Clinical Research Associate, Sponsor Dedicated

Perform site monitoring visits, work with sites to adapt, drive, and track subject recruitment plan, and manage the progress of assigned studies to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Requirements

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