Site Visit Report Reviewer
Core
Reviewing clinical trial site visit reports to ensure compliance with regulatory standards and internal SOPs.
Role type
Clinical trial documentation reviewer
Builds
Compliance-aligned clinical research data
Domain
Clinical research / Healthcare
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
ICH-GCP guidelines knowledge, clinical trial process understanding, attention to detail, issue tracking, regulatory compliance standards
Preferred skills
Experience in site management or clinical research, analytical thinking, problem-solving
Technologies
Microsoft Office
Responsibilities
Review site visit reports (qualification, initiation, monitoring, termination) for compliance; Track and follow up on open issues, protocol deviations, and adverse events; Collaborate with CRAs and Clinical Operations Leaders; Conduct quality checks on Monitoring Visit Reports; Support periodic analysis of monitoring activities
Seniority
Individual Contributor