Clinical Research Monitoring Specialist

Role Overview

• Field monitoring of studies and data collection for clinical trials
• Assessing all data documentation, reports, records, transcripts, exam results for consistency with case report form
• Verifying trial/study data and maintaining appropriate regulatory documents
• Providing oversight of and insights into trial activities to principal investigators and support staff
• Developing and delivering training on GCPs, protocols, database, compliance, device accountability, adverse event reporting

Requirements

• Bachelor's Degree or equivalent in related field
• 3 years of field monitoring, quality assurance/control and regulatory compliance experience or equivalent work experience based on Edwards criteria
• Ability to travel up to 75% domestically

Benefits

• Competitive salaries
• Performance-based incentives
• A wide variety of benefits programs to address diverse individual needs
• Health insurance
• Retirement plans
• Paid time off
• Professional development