(Senior) Clinical Research Associate (CRA)

Perform monitoring and site management work 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. Conduct site visits, manage ongoing project expectations and issues, and evaluate the quality and integrity of study site practices.

Requirements

• Bachelor's Degree in scientific discipline or health care
• At least 1 year of on-site monitoring experience
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements
• Good therapeutic and protocol knowledge
• 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
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients

Benefits

• Professional development opportunities
• Competitive salary and benefits
• Opportunities for career advancement