Clinical Research Associate 2
Core
Partner with investigators and site staff to ensure appropriate conduct of clinical trials, driving data integrity, compliance, and study performance.
Role type
Senior Clinical Research Associate (Site Monitoring)
Builds
Clinical trial execution and data integrity for investigational drugs/devices
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Site evaluation and monitoring, protocol compliance, risk assessment, patient recruitment and retention, site engagement strategy, regulatory knowledge (ICH/GCP), mentorship of junior CRAs
Preferred skills
Tertiary qualification in health-related disciplines, therapeutic area knowledge, risk-based monitoring approach
Technologies
CRM tools
Responsibilities
Conduct site evaluation, training, routine, and closure monitoring; align and train site staff on trial goals; ensure audit and regulatory inspection readiness; manage investigator payments; identify and evaluate potential investigators/sites; resolve site risk signals and implement corrective actions; ensure quality and timely submission of data and safety reports.
Seniority
Mid-Senior, hands-on IC with mentorship responsibilities