The Site-ICRA I is responsible for supporting site management activities such as collection and review of essential regulatory documents and clinical inventory management
Job Summary
The Site-ICRA I is responsible for supporting site management activities such as collection and review of essential regulatory documents and clinical inventory management.
This role involves collaboration with US and EMEA Clinical Site Operations teams and maintaining compliance with Good Clinical Practice and Good Documentation Practice standards.
The position requires strong communication skills and proficiency in Microsoft Office, with opportunities to contribute to global or regional process improvements.
Matching Summary
The Site-ICRA I is responsible for supporting site management activities such as collection and review of essential regulatory documents and clinical inventory management.
Skills & Requirements
Must-have
Review and analyze regulatory documents
Clinical inventory management
Good Clinical Practice (GCP) compliance
Document management systems
Microsoft Office Suite proficiency
Collaboration with global teams
Nice-to-have
Strong written and verbal communication
Organizational and analytical skills
Ability to work independently
Familiarity with clinical trial processes
Attention to detail
Presentation skills
Key Requirements
Bachelor’s degree in natural science or related field
Minimum two years of relevant experience
Certification by SoCRA or ACRP preferred
Knowledge of clinical regulations and industry practices