Clinical Research

• Deliver clinical trial monitoring work to a high standard
• Work closely with the team and stakeholders
• Ensure studies are conducted according to study protocols, operating procedures, and good clinical practice
• Validate product performance claims
• Supply data for critical Regulatory submissions
• Define the functional and clinical utility of investigation products
• Understand and implement federal regulations
• Help roll out SOPs to ensure studies adhere to FDA regulations, GCP, IVD directives, and client policy
• Contribute to designing, planning, coordinating, and conducting activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics

Explore Clinical Research Associate – Level 1 at ICON plc. Review requirements and application details.

Clinical Research Associate – Level 1

Clinical Study Manager

Senior Clinical Data Manager – Data Standards

Principal Biostatistician, Senior Biostatistician – R/Rshiny

Business Development Director – Clinical Research

Clinical Trial Manager I/II

Clinical Data Manager

Clinical Trial Manager – Regulatory Submissions

Senior Biostatistician – Biomarker Experience

Biostatistician – Biomarker Experience