CRA (Level II)
Core
Conducts remote or on-site clinical monitoring and site management to ensure protocol and regulatory compliance, manage documentation, and guarantee subject rights and data reliability.
Role type
Clinical Research Associate (Level II)
Builds
Clinical trial operations
Domain
Healthcare / Clinical Research
Deliverable
physical/clinical work
Required skills
Clinical monitoring, site management, protocol compliance, regulatory compliance, documentation management, audit readiness, ICH-GCP knowledge, SOP adherence
Responsibilities
Conduct remote or on-site visits to assess protocol and regulatory compliance, manage procedures and guidelines from different sponsors, develop collaborative relationships with investigational sites, ensure audit readiness
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