Senior Clinical Research Associate
Core
Independently manage and oversee site management and monitoring activities during clinical trial execution for medical devices treating Afib and related conditions.
Role type
Senior Clinical Research Associate (Site Management & Monitoring)
Builds
Clinical trial data integrity and regulatory compliance for medical device studies
Domain
Medical Devices / Clinical Research
Required skills
Site qualification, protocol adherence, data query resolution, regulatory compliance, training facilitation, cross-functional liaison
Preferred skills
Leadership of junior team members, adapting to evolving study needs
Technologies
EDC systems, clinical trial protocols
Responsibilities
Coordinate collection and review of essential documents from clinical investigation sites; Conduct Site Qualification, Initiation, Interim and Close-Out training visits; Act as primary point of contact for site communications and inquiries; Ensure clinical study sites adhere to assigned protocols and regulatory standards; Review and analyze data for accuracy and completeness; Lead the creation, management, and resolution of data queries for assigned sites
