CRA Level I
Core
Conduct remote or on-site clinical monitoring and site management to ensure trials comply with protocols, ICH-GCP guidelines, and regulations.
Role type
Junior Clinical Research Associate (IC)
Builds
Clinical trial data and compliance documentation for pharmaceutical and biotech sponsors
Domain
Life Sciences / Clinical Research
Required skills
Clinical monitoring, regulatory compliance, ICH-GCP guidelines, site management, medical terminology, audit readiness, documentation management
Preferred skills
None stated
Technologies
None stated
Responsibilities
Conduct remote or on-site visits to assess protocol and regulatory compliance; Manage procedures and guidelines from different sponsors; Ensure audit readiness; Develop collaborative relationships with investigational sites
Seniority
Junior, entry-level IC
