Clinical Research Associate (CRA) - All Levels
Core
Conducts remote or on-site monitoring of clinical trial sites to ensure protocol and regulatory compliance, manage documentation, and guarantee data reliability and subject safety.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data and compliance for sponsors/government clients
Domain
Clinical research / Life sciences
Deliverable
physical/clinical work
Required skills
Risk-based monitoring, Root cause analysis, Protocol compliance, ICH-GCP knowledge, Regulatory compliance, Data review (SDR/SDV/CRF), Site management, Investigational product inventory, Medical terminology
Preferred skills
Therapeutic area knowledge, Problem-solving, Team collaboration, Time management, Microsoft Office
Technologies
Clinical Trial Management Systems, Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches; Conduct on-site and remote monitoring visits; Review data and documents for accuracy; Manage investigational product inventory; Ensure audit readiness; Facilitate communication between sites, clients, and internal teams; Perform trial close-out and material retrieval.
Seniority
All levels (entry to experienced)