About this role
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance and data integrity while collaborating with investigators to maintain high-quality clinical data.
Candidates must have a bachelor's degree in a scientific or healthcare field and at least 2 years of experience as a Clinical Research Associate. Proficiency in ICH-GCP guidelines and the ability to travel at least 60% of the time are required.
What they're looking for
Site QualificationSite InitiationClinical MonitoringProtocol ComplianceData IntegrityPatient SafetyData ReviewQuery Resolution
Frequently asked questions
What does a CRA II at ICON plc do?
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance and data integrity while collaborating with investigators to maintain high-quality clinical data. Candidates must have a bachelor's degree in…
What skills does this CRA II role need?
Key skills for this role include Site Qualification, Site Initiation, Clinical Monitoring, Protocol Compliance, Data Integrity, Patient Safety.
How much does a CRA II at ICON plc pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this CRA II role remote, hybrid, or on-site?
This role is remote ok, based in Singapore.
How do I apply for this CRA II role?
You can apply directly on ICON plc's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.