Clinical Research Associate
Core
Conducting clinical monitoring visits, training site staff, and managing complex clinical studies to ensure data quality and regulatory compliance.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and site compliance for medical science studies
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Preparation and conduct of monitoring visits (selection, initiation, routine, closeout), CRF review, source document verification, query resolution, site communication and management, feasibility research, presentation delivery, regulatory document procurement support, automated tracking system maintenance
Preferred skills
Experience in Clinical Research, training and mentoring others, planning in dynamic team environments
Technologies
MS Office applications, study-specific automated tracking systems
Responsibilities
Conduct selection, initiation, routine, and closeout monitoring visits; Deliver training to investigators and site staff; Perform CRF review and source document verification; Manage site communication and identification; Participate in feasibility research and investigator meetings; Prepare for and resolve audit findings; Support Regulatory Affairs with document procurement; Maintain study-specific tracking systems
Seniority
Senior, hands-on IC with mentorship responsibilities