Clinical Research Monitoring Specialist
Edwards Lifesciences
full-time
Posted on:
Location Type: Hybrid
Location: Boston • Massachusetts • United States
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Salary
💰 $87,000 - $123,000 per year
About the role
- 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
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
data collectiondata documentationquality assuranceregulatory complianceGCPsprotocolsadverse event reportingdevice accountabilityfield monitoring
Soft Skills
oversightcommunicationtraininginsightorganizational
Certifications
Bachelor's Degree