FSP Bench Clinical Research Associate I
Core
Monitors clinical trial investigator sites using risk-based approaches to ensure compliance with protocols and regulations, verify data accuracy, and manage investigational product inventory.
Role type
Junior Clinical Research Associate (Site Monitoring)
Builds
Clinical trial sites and compliant data sets for pharmaceutical/biotech clients
Domain
Clinical Research / Life Sciences
Required skills
Risk-based monitoring, Root cause analysis (RCA), Data Source Verification (SDV), Critical thinking, Regulatory compliance (ICH-GCP), Investigational product inventory management, Report writing, Issue escalation, Site initiation, Trial close-out, Travel management
Preferred skills
None stated
Technologies
Clinical Trial Management Systems (CTMS)
Responsibilities
Monitor investigator sites for protocol and regulatory compliance, verify data accuracy through on-site and remote activities, assess investigational product inventory, initiate and close out clinical trial sites, track trial status and progress, facilitate communication between sites, clients, and internal teams, respond to audits and inspections, complete administrative tasks like expense reports and timesheets.
Seniority
Junior, hands-on IC