(Senior) Clinical Research Associate
Core
Lead and execute site monitoring visits to ensure clinical trials are executed with excellence, compliance, and patient focus.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trials
Domain
Life sciences / Healthcare
Deliverable
physical/clinical work
Required skills
Site monitoring, GCP/ICH compliance, Data integrity management, Risk identification, Study progress tracking, Regulatory approval management
Preferred skills
Relationship building with investigative sites, Multi-priority management
Responsibilities
Lead site monitoring visits (selection, initiation, routine, close-out), Drive site performance and recruitment, Ensure protocol compliance and data quality, Identify and resolve study risks, Track study progress and regulatory approvals, Maintain documentation for inspection readiness
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