Clinical Research Associate - Experienced II/Sr
Core
Conduct on-site and remote monitoring visits to clinical trial sites to ensure compliance with protocols, regulations, and quality standards.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial operations and data integrity
Domain
Clinical research / Healthcare
Required skills
Clinical trial monitoring, regulatory compliance, site relationship management, study documentation review, corrective and preventive action (CAPA), clinical protocol adherence, risk identification, travel for site visits
Preferred skills
Experience with virtual and in-person team collaboration, adaptability in fast-paced environments
Technologies
Clinical trial management systems
Responsibilities
Conduct on-site and remote monitoring visits, manage site-level clinical trial documentation, prepare monitoring visit reports, identify deviations and implement corrective actions, maintain audit-ready sites, communicate findings to stakeholders
Seniority
Senior, hands-on IC