Clinical Trial Associate I
Core
Supports Project Managers and study teams in conducting clinical ophthalmic projects, ensuring compliance with GCP protocols and managing site regulatory documentation.
Role type
Junior Clinical Trial Associate (CTA I)
Builds
Clinical study documentation, regulatory packages, and site support materials for ophthalmic drug and device development.
Domain
Clinical Research / Ophthalmics
Deliverable
client delivery
Required skills
GCP/ICH regulations knowledge, regulatory document management, site coordination, electronic Trial Master File (eTMF) maintenance, audit support, project tracking
Preferred skills
Ophthalmic experience, 1+ years clinical trial experience, multilingual communication
Technologies
eTMF systems, CTMS, Box.com, Z:drive
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