Edwards Lifesciences
Senior Specialist, Clinical Research Monitoring
USA-Georgia-Remote · Senior
Sponsorship not specified$108k-$153kDetected 8 days ago
GCPComplianceExcelAuditingClinical TrialsClinical ResearchPatient CarePharmacovigilanceMedical DevicesResearchLeadershipCommunicationProblem SolvingCritical ThinkingWritingMicrosoft Office
About the role
- We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients' lives.
Requirements
- Bachelor's Degree or equivalent in related field with 5 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.
Skills
- Imagine how your ideas and expertise can change a patient's life.
- Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and under-treated.
- It's our driving force to help patients live longer and healthier lives.
- Contributing to the development of clinical protocols, informed consent forms, and case report forms.
- Editing/amending informed consent documents.
Compensation
- The base pay range for this position is $108,000 to $153,000 (highly experienced).
Benefits
- Moderate understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
Visa & Work Authorization
- ol compliance, enrollment, monitoring deviations, data quality) to principal investigators and support staff, and study sponsor management and leadership staff, including Institutional Review Boards/Ethics Committees/Res
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This listing is sourced directly from Edwards Lifesciences's careers page and normalized into a canonical job model.