Senior Specialist, Clinical Research Monitoring

Role Overview

• Field monitoring of studies and data collection for clinical trials
• Assessing all data documentation, reports, records, transcripts, exam results for consistency
• Developing and delivering technical training on GCPs and other relevant protocols
• Acting as a mentor to new or junior level employees
• Providing oversight of trial activities to principal investigators and support staff
• Validating investigational device accountability by tracking devices from Edwards to field sites
• Verifying trial/study data and maintaining appropriate regulatory documents

Requirements

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

Benefits

• Competitive salaries
• Performance-based incentives
• Wide variety of benefits programs to address diverse individual needs