Clinical Research Associate II - MedTech

IQVIA · Washington, DC

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Clinical OperationsFull-time$90k–$150kCompany career page

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Role summary

IQVIA MedTech seeks a Clinical Research Associate II to conduct site monitoring and management for medical device and diagnostic studies. The role ensures protocol compliance, regulatory adherence, and data integrity across assigned clinical trial sites.

What they're looking for

Bachelor's degree in scientific or healthcare discipline preferred
Minimum 1 year of on-site clinical trial monitoring experience
Strong knowledge of GCP and ICH guidelines
Proficiency with Microsoft Office and laptop/mobile devices
Excellent written and verbal English communication skills
Strong organizational and problem-solving abilities

What you'll be doing

Conduct site monitoring visits including initiation, ongoing monitoring, and close-out according to protocol and regulatory standards
Partner with sites on subject recruitment planning and tracking to meet enrollment targets
Deliver protocol training and maintain regular communication with sites regarding compliance and expectations
Evaluate site practices for protocol adherence and data quality; escalate issues as needed
Track study progress including regulatory approvals, enrollment metrics, CRF completion, and data queries

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