Associate Clinical Research Associate
Core
Primary site contact and manager for clinical research studies, ensuring high-quality trial execution, compliance, and patient safety across all phases.
Role type
Associate Clinical Research Associate (CRA)
Builds
Clinical research studies for pharmaceutical/biotech sponsors
Domain
Healthcare / Clinical Research
Deliverable
physical/clinical work
Required skills
Clinical research methods, Clinical site management, Clinical study management, Clinical trials monitoring, GCP/ICH standards, Good Documentation Practices, Regulatory documentation management, Data quality maintenance, Root cause analysis, Corrective and preventive actions
Preferred skills
Site performance management, Patient recruitment, Remote monitoring, Basic automation and analytics, AI tools usage
Technologies
CTMS, eTMF, MS Office, Clinical applications on desktop/tablet/mobile
Responsibilities
Perform remote and on-site monitoring (initiation, validation, monitoring, close-out), Coordinate site readiness with internal teams, Prepare visit and non-visit reports, Collect and review regulatory documentation, Identify and resolve site performance/compliance issues, Support audit and inspection activities, Travel 65-75% of working time domestically and internationally
Seniority
Associate, hands-on IC
