Clinical Research Associate
On-siteNo visa sponsorship
Core
Supports Global Clinical Operations by coordinating site regulatory submissions, managing essential documents, and ensuring investigator readiness for clinical trials.
Role type
Clinical Research Associate
Builds
Clinical trial operations and regulatory compliance
Domain
Medical devices / Clinical Research
Deliverable
client delivery
Required skills
Regulatory document management, Site start-up coordination, Informed Consent Form (ICF) customization, Clinical Trial Management Systems (CTMS), Electronic Trial Master File (eTMF), ICH/GCP compliance, IRB/EC approval tracking, Quality audit support
Preferred skills
None stated
Technologies
Clinical Trial Management Systems, eTMF
